Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
---|
HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | AAGAB CL E G H | 79719 | 25662 | ORPHA:79501 | Punctate palmoplantar keratoderma type 1 | | | | 7 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | ADA2 CL E G H | 51816 | 1839 | ORPHA:124 | Blackfan-Diamond anemia | | | | 22 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | AKT1 CL E G H | 207 | 391 | OMIM:114500 | Colorectal cancer | | | | 54 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | AKT1 CL E G H | 207 | 391 | ORPHA:201 | Cowden syndrome | | | | 54 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | APC CL E G H | 324 | 583 | OMIM:175100 | Adenomatous polyposis coli | | | | 3179 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | APC CL E G H | 324 | 583 | ORPHA:247806 | APC-related attenuated familial adenomatous polyposis | | | | 3179 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | APC CL E G H | 324 | 583 | OMIM:114500 | Colorectal cancer | | | | 3179 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | APC CL E G H | 324 | 583 | OMIM:135290 | Desmoid disease, hereditary | | | | 3179 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | APC CL E G H | 324 | 583 | ORPHA:261584 | Familial adenomatous polyposis due to 5q22.2 microdeletion | | | | 3179 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | APC CL E G H | 324 | 583 | ORPHA:79665 | Gardner syndrome | | | | 3179 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | APC CL E G H | 324 | 583 | ORPHA:99818 | Turcot syndrome with polyposis | | | | 3179 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | AURKA CL E G H | 6790 | 11393 | OMIM:114500 | Colorectal cancer | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | AXIN2 CL E G H | 8313 | 904 | ORPHA:401911 | AXIN2-related attenuated familial adenomatous polyposis | | | | 435 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | AXIN2 CL E G H | 8313 | 904 | OMIM:114500 | Colorectal cancer | | | | 435 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | AXIN2 CL E G H | 8313 | 904 | OMIM:608615 | OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS | | | | 435 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BAX CL E G H | 581 | 959 | OMIM:114500 | Colorectal cancer | | | | 4 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BLM CL E G H | 641 | 1058 | ORPHA:125 | Bloom syndrome | | | | 314 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BMPR1A CL E G H | 657 | 1076 | ORPHA:440437 | Familial colorectal cancer Type X | | | | 385 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BMPR1A CL E G H | 657 | 1076 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | | | | 385 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BMPR1A CL E G H | 657 | 1076 | ORPHA:157794 | Hereditary mixed polyposis syndrome | | | | 385 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BMPR1A CL E G H | 657 | 1076 | ORPHA:79076 | Juvenile polyposis of infancy | | | | 385 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BMPR1A CL E G H | 657 | 1076 | OMIM:174900 | Juvenile polyposis syndrome | | | | 385 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BMPR1A CL E G H | 657 | 1076 | OMIM:610069 | POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2 | | | | 385 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BRAF CL E G H | 673 | 1097 | OMIM:114500 | Colorectal cancer | | | | 276 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BRCA1 CL E G H | 672 | 1100 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 5769 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BRCA2 CL E G H | 675 | 1101 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 7642 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BUB1 CL E G H | 699 | 1148 | OMIM:114500 | Colorectal cancer | | | | 5 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BUB1 CL E G H | 699 | 1148 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | | | | 5 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BUB1B CL E G H | 701 | 1149 | OMIM:114500 | Colorectal cancer | | | | 76 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BUB1B CL E G H | 701 | 1149 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | | | | 76 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | BUB3 CL E G H | 9184 | 1151 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | | | | | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | CCND1 CL E G H | 595 | 1582 | OMIM:114500 | Colorectal cancer | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 289 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:524 | Li-Fraumeni syndrome | | | | 289 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | CEP57 CL E G H | 9702 | 30794 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | | | | 17 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | CHEK2 CL E G H | 11200 | 16627 | OMIM:114500 | Colorectal cancer | | | | 833 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | CHEK2 CL E G H | 11200 | 16627 | ORPHA:524 | Li-Fraumeni syndrome | | | | 833 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | COL14A1 CL E G H | 7373 | 2191 | ORPHA:79501 | Punctate palmoplantar keratoderma type 1 | | | | 2 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | CTNNB1 CL E G H | 1499 | 2514 | OMIM:114500 | Colorectal cancer | | | | 88 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | DCC CL E G H | 1630 | 2701 | OMIM:114500 | Colorectal cancer | | | | 36 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | DICER1 CL E G H | 23405 | 17098 | ORPHA:276399 | Familial multinodular goiter | | | | 670 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | DLC1 CL E G H | 10395 | 2897 | OMIM:114500 | Colorectal cancer | | | | 11 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | DOCK8 CL E G H | 81704 | 19191 | ORPHA:217390 | Combined immunodeficiency due to DOCK8 deficiency | | | | 217 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | ENG CL E G H | 2022 | 3349 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | | | | 186 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | EP300 CL E G H | 2033 | 3373 | OMIM:114500 | Colorectal cancer | | | | 250 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | EPCAM CL E G H | 4072 | 11529 | OMIM:613244 | Colorectal cancer, hereditary nonpolyposis, type 8 | | | | 170 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | EPCAM CL E G H | 4072 | 11529 | ORPHA:144 | Lynch syndrome | | | | 170 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | FAN1 CL E G H | 22909 | 29170 | ORPHA:144 | Lynch syndrome | | | | 15 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | FGFR3 CL E G H | 2261 | 3690 | OMIM:114500 | Colorectal cancer | | | | 145 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | FLCN CL E G H | 201163 | 27310 | OMIM:135150 | Birt-Hogg-Dube syndrome | | | | 332 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | FLCN CL E G H | 201163 | 27310 | OMIM:114500 | Colorectal cancer | | | | 332 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | FOXE1 CL E G H | 2304 | 3806 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | | | | 9 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | GATA1 CL E G H | 2623 | 4170 | ORPHA:124 | Blackfan-Diamond anemia | | | | 29 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | GPR35 CL E G H | 2859 | 4492 | ORPHA:171 | Primary sclerosing cholangitis | | | | 2 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | GREM1 CL E G H | 26585 | 2001 | ORPHA:157794 | Hereditary mixed polyposis syndrome | | | | 9 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | HABP2 CL E G H | 3026 | 4798 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | | | | 58 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | KEAP1 CL E G H | 9817 | 23177 | ORPHA:276399 | Familial multinodular goiter | | | | | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | KIT CL E G H | 3815 | 6342 | ORPHA:44890 | Gastrointestinal stromal tumor | | | | 327 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | KLLN CL E G H | 100144748 | 37212 | ORPHA:201 | Cowden syndrome | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | KRAS CL E G H | 3845 | 6407 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 196 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | KRAS CL E G H | 3845 | 6407 | ORPHA:144 | Lynch syndrome | | | | 196 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MBD4 CL E G H | 8930 | 6919 | OMIM:619975 | | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MCC CL E G H | 4163 | 6935 | OMIM:114500 | Colorectal cancer | | | | 6 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MDM2 CL E G H | 4193 | 6973 | ORPHA:524 | Li-Fraumeni syndrome | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MINPP1 CL E G H | 9562 | 7102 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | | | | 3 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MLH1 CL E G H | 4292 | 7127 | OMIM:609310 | COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2; HNPCC2 | | | | 1819 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MLH1 CL E G H | 4292 | 7127 | ORPHA:144 | Lynch syndrome | | | | 1819 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MLH1 CL E G H | 4292 | 7127 | OMIM:276300 | Mismatch repair cancer syndrome 1 | | | | 1819 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MLH1 CL E G H | 4292 | 7127 | ORPHA:587 | Muir-Torre syndrome | | | | 1819 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MLH1 CL E G H | 4292 | 7127 | OMIM:158320 | Muir-Torre syndrome | | | | 1819 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MLH3 CL E G H | 27030 | 7128 | OMIM:114500 | Colorectal cancer | | | | 131 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MLH3 CL E G H | 27030 | 7128 | OMIM:614385 | Colorectal cancer, hereditary nonpolyposis, type 7 | | | | 131 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MLH3 CL E G H | 27030 | 7128 | ORPHA:144 | Lynch syndrome | | | | 131 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH2 CL E G H | 4436 | 7325 | ORPHA:144 | Lynch syndrome | | | | 2162 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH2 CL E G H | 4436 | 7325 | OMIM:120435 | Lynch syndrome I | | | | 2162 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH2 CL E G H | 4436 | 7325 | OMIM:619096 | MISMATCH REPAIR CANCER SYNDROME 2; MMRCS2 | | | | 2162 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH2 CL E G H | 4436 | 7325 | OMIM:158320 | Muir-Torre syndrome | | | | 2162 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH2 CL E G H | 4436 | 7325 | ORPHA:587 | Muir-Torre syndrome | | | | 2162 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH3 CL E G H | 4437 | 7326 | OMIM:617100 | Familial adenomatous polyposis 4 | | | | 5 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH3 CL E G H | 4437 | 7326 | ORPHA:480536 | MSH3-related attenuated familial adenomatous polyposis | | | | 5 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH6 CL E G H | 2956 | 7329 | OMIM:614350 | Colorectal cancer, hereditary nonpolyposis, type 5 | | | | 2232 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH6 CL E G H | 2956 | 7329 | ORPHA:144 | Lynch syndrome | | | | 2232 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH6 CL E G H | 2956 | 7329 | OMIM:619097 | MISMATCH REPAIR CANCER SYNDROME 3; MMRCS3 | | | | 2232 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MSH6 CL E G H | 2956 | 7329 | ORPHA:587 | Muir-Torre syndrome | | | | 2232 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MST1 CL E G H | 4485 | 7380 | ORPHA:171 | Primary sclerosing cholangitis | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MUTYH CL E G H | 4595 | 7527 | OMIM:608456 | Familial adenomatous polyposis, 2 | | | | 592 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | MUTYH CL E G H | 4595 | 7527 | ORPHA:247798 | MUTYH-related attenuated familial adenomatous polyposis | | | | 592 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | NRAS CL E G H | 4893 | 7989 | OMIM:114500 | Colorectal cancer | | | | 102 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | NTHL1 CL E G H | 4913 | 8028 | OMIM:616415 | Familial adenomatous polyposis 3 | | | | 2 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | NTHL1 CL E G H | 4913 | 8028 | ORPHA:454840 | NTHL1-related attenuated familial adenomatous polyposis | | | | 2 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PALB2 CL E G H | 79728 | 26144 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 1349 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PALLD CL E G H | 23022 | 17068 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 192 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PDE11A CL E G H | 50940 | 8773 | ORPHA:1359 | Carney complex | | | | 13 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PDGFRA CL E G H | 5156 | 8803 | ORPHA:44890 | Gastrointestinal stromal tumor | | | | 337 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PDGFRL CL E G H | 5157 | 8805 | OMIM:114500 | Colorectal cancer | | | | 2 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PIK3CA CL E G H | 5290 | 8975 | OMIM:114500 | Colorectal cancer | | | | 162 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:201 | Cowden syndrome | | | | 162 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:144 | Lynch syndrome | | | | 162 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PLA2G2A CL E G H | 5320 | 9031 | OMIM:114500 | Colorectal cancer | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PMS1 CL E G H | 5378 | 9121 | ORPHA:144 | Lynch syndrome | | | | 56 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PMS1 CL E G H | 5378 | 9121 | OMIM:120435 | Lynch syndrome I | | | | 56 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PMS2 CL E G H | 5395 | 9122 | OMIM:614337 | Colorectal cancer, hereditary nonpolyposis, type 4 | | | | 1121 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PMS2 CL E G H | 5395 | 9122 | ORPHA:144 | Lynch syndrome | | | | 1121 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PMS2 CL E G H | 5395 | 9122 | OMIM:619101 | MISMATCH REPAIR CANCER SYNDROME 4; MMRCS4 | | | | 1121 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | POLD1 CL E G H | 5424 | 9175 | OMIM:612591 | Colorectal cancer, susceptibility to, 10 | | | | 731 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | POLD1 CL E G H | 5424 | 9175 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | | | | 731 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | POLE CL E G H | 5426 | 9177 | OMIM:615083 | Colorectal cancer, susceptibility to, 12 | | | | 1129 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | POLE CL E G H | 5426 | 9177 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | | | | 1129 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PRKAR1A CL E G H | 5573 | 9388 | ORPHA:1359 | Carney complex | | | | 134 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PTEN CL E G H | 5728 | 9588 | ORPHA:201 | Cowden syndrome | | | | 948 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PTEN CL E G H | 5728 | 9588 | ORPHA:79076 | Juvenile polyposis of infancy | | | | 948 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PTPN12 CL E G H | 5782 | 9645 | OMIM:114500 | Colorectal cancer | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | PTPRJ CL E G H | 5795 | 9673 | OMIM:114500 | Colorectal cancer | | | | 3 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RABL3 CL E G H | 285282 | 18072 | ORPHA:1333 | Familial pancreatic carcinoma | | | | | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RAD54B CL E G H | 25788 | 17228 | OMIM:114500 | Colorectal cancer | | | | 2 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RNF43 CL E G H | 54894 | 18505 | ORPHA:157798 | Serrated polyposis syndrome | HP:0040283 - Occasional | | | 5 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPL11 CL E G H | 6135 | 10301 | ORPHA:124 | Blackfan-Diamond anemia | | | | 22 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPL15 CL E G H | 6138 | 10306 | ORPHA:124 | Blackfan-Diamond anemia | | | | 3 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPL18 CL E G H | 6141 | 10310 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPL26 CL E G H | 6154 | 10327 | ORPHA:124 | Blackfan-Diamond anemia | | | | 3 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPL27 CL E G H | 6155 | 10328 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPL31 CL E G H | 6160 | 10334 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPL35 CL E G H | 11224 | 10344 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPL35A CL E G H | 6165 | 10345 | ORPHA:124 | Blackfan-Diamond anemia | | | | 11 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPL5 CL E G H | 6125 | 10360 | ORPHA:124 | Blackfan-Diamond anemia | | | | 40 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS10 CL E G H | 6204 | 10383 | ORPHA:124 | Blackfan-Diamond anemia | | | | 26 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS15A CL E G H | 6210 | 10389 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS17 CL E G H | 6218 | 10397 | ORPHA:124 | Blackfan-Diamond anemia | | | | 5 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS19 CL E G H | 6223 | 10402 | ORPHA:124 | Blackfan-Diamond anemia | | | | 42 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS19 CL E G H | 6223 | 10402 | OMIM:105650 | Diamond-Blackfan anemia 1 | | | | 42 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS20 CL E G H | 6224 | 10405 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS20 CL E G H | 6224 | 10405 | ORPHA:440437 | Familial colorectal cancer Type X | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS24 CL E G H | 6229 | 10411 | ORPHA:124 | Blackfan-Diamond anemia | | | | 22 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS26 CL E G H | 6231 | 10414 | ORPHA:124 | Blackfan-Diamond anemia | | | | 20 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS27 CL E G H | 6232 | 10416 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS28 CL E G H | 6234 | 10418 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS29 CL E G H | 6235 | 10419 | ORPHA:124 | Blackfan-Diamond anemia | | | | 3 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | RPS7 CL E G H | 6201 | 10440 | ORPHA:124 | Blackfan-Diamond anemia | | | | 20 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SDHA CL E G H | 6389 | 10680 | ORPHA:44890 | Gastrointestinal stromal tumor | | | | 304 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SDHB CL E G H | 6390 | 10681 | ORPHA:201 | Cowden syndrome | | | | 237 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SDHB CL E G H | 6390 | 10681 | ORPHA:44890 | Gastrointestinal stromal tumor | | | | 237 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SDHC CL E G H | 6391 | 10682 | ORPHA:201 | Cowden syndrome | | | | 147 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SDHC CL E G H | 6391 | 10682 | ORPHA:44890 | Gastrointestinal stromal tumor | | | | 147 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SDHD CL E G H | 6392 | 10683 | ORPHA:201 | Cowden syndrome | | | | 129 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SEC23B CL E G H | 10483 | 10702 | ORPHA:201 | Cowden syndrome | | | | 60 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SEMA4A CL E G H | 64218 | 10729 | ORPHA:440437 | Familial colorectal cancer Type X | | | | 48 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SEMA4D CL E G H | 10507 | 10732 | ORPHA:171 | Primary sclerosing cholangitis | | | | | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SH3KBP1 CL E G H | 30011 | 13867 | OMIM:300310 | Immunodeficiency 61 | | | | 2 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SMAD4 CL E G H | 4089 | 6770 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 504 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SMAD4 CL E G H | 4089 | 6770 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | | | | 504 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SMAD4 CL E G H | 4089 | 6770 | OMIM:174900 | Juvenile polyposis syndrome | | | | 504 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SMAD7 CL E G H | 4092 | 6773 | OMIM:612229 | Caudal duplication anomaly | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | SRC CL E G H | 6714 | 11283 | OMIM:114500 | Colorectal cancer | | | | 15 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | STK11 CL E G H | 6794 | 11389 | ORPHA:2869 | Peutz-Jeghers syndrome | | | | 740 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | TCF4 CL E G H | 6925 | 11634 | ORPHA:171 | Primary sclerosing cholangitis | | | | 241 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | TGFBR2 CL E G H | 7048 | 11773 | OMIM:614331 | COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6; HNPCC6 | | | | 253 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | TGFBR2 CL E G H | 7048 | 11773 | ORPHA:144 | Lynch syndrome | | | | 253 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | TLR2 CL E G H | 7097 | 11848 | OMIM:114500 | Colorectal cancer | | | | 5 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | TP53 CL E G H | 7157 | 11998 | OMIM:114500 | Colorectal cancer | | | | 911 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | TP53 CL E G H | 7157 | 11998 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 911 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | TP53 CL E G H | 7157 | 11998 | OMIM:151623 | Li-Fraumeni syndrome | | | | 911 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | TP53 CL E G H | 7157 | 11998 | ORPHA:524 | Li-Fraumeni syndrome | | | | 911 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | TRIP13 CL E G H | 9319 | 12307 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | | | | 2 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | TSR2 CL E G H | 90121 | 25455 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0100834 | Neoplasm of the large intestine | 0 | USF3 CL E G H | 205717 | 30494 | ORPHA:201 | Cowden syndrome | | | | 1 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | AAGAB CL E G H | 79719 | 25662 | ORPHA:79501 | Punctate palmoplantar keratoderma type 1 | | | | 7 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | AAGAB CL E G H | 79719 | 25662 | ORPHA:79501 | Punctate palmoplantar keratoderma type 1 | | | | 7 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | ADA2 CL E G H | 51816 | 1839 | ORPHA:124 | Blackfan-Diamond anemia | | | | 22 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | ADA2 CL E G H | 51816 | 1839 | ORPHA:124 | Blackfan-Diamond anemia | | | | 22 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | AKT1 CL E G H | 207 | 391 | OMIM:114500 | Colorectal cancer | . | | | 54 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | AKT1 CL E G H | 207 | 391 | ORPHA:201 | Cowden syndrome | | | | 54 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | APC CL E G H | 324 | 583 | OMIM:175100 | Adenomatous polyposis coli | | | | 3179 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | APC CL E G H | 324 | 583 | ORPHA:247806 | APC-related attenuated familial adenomatous polyposis | | | | 3179 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | APC CL E G H | 324 | 583 | OMIM:114500 | Colorectal cancer | . | | | 3179 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | APC CL E G H | 324 | 583 | OMIM:135290 | Desmoid disease, hereditary | | | | 3179 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | APC CL E G H | 324 | 583 | OMIM:135290 | Desmoid disease, hereditary | | | | 3179 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | APC CL E G H | 324 | 583 | ORPHA:261584 | Familial adenomatous polyposis due to 5q22.2 microdeletion | | | | 3179 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | APC CL E G H | 324 | 583 | ORPHA:79665 | Gardner syndrome | | | | 3179 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | APC CL E G H | 324 | 583 | ORPHA:99818 | Turcot syndrome with polyposis | | | | 3179 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | AURKA CL E G H | 6790 | 11393 | OMIM:114500 | Colorectal cancer | . | | | 1 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | AXIN2 CL E G H | 8313 | 904 | ORPHA:401911 | AXIN2-related attenuated familial adenomatous polyposis | HP:0040283 - Occasional | | | 435 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | AXIN2 CL E G H | 8313 | 904 | ORPHA:401911 | AXIN2-related attenuated familial adenomatous polyposis | | | | 435 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | AXIN2 CL E G H | 8313 | 904 | OMIM:114500 | Colorectal cancer | . | | | 435 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | AXIN2 CL E G H | 8313 | 904 | OMIM:608615 | OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS | | | | 435 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | BAX CL E G H | 581 | 959 | OMIM:114500 | Colorectal cancer | . | | | 4 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BLM CL E G H | 641 | 1058 | ORPHA:125 | Bloom syndrome | HP:0040283 - Occasional | | | 314 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BMPR1A CL E G H | 657 | 1076 | ORPHA:440437 | Familial colorectal cancer Type X | HP:0040283 - Occasional | | | 385 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | BMPR1A CL E G H | 657 | 1076 | ORPHA:440437 | Familial colorectal cancer Type X | HP:0040282 - Frequent | | | 385 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | BMPR1A CL E G H | 657 | 1076 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | | | | 385 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BMPR1A CL E G H | 657 | 1076 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | | | | 385 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | BMPR1A CL E G H | 657 | 1076 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040283 - Occasional | | | 385 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BMPR1A CL E G H | 657 | 1076 | ORPHA:157794 | Hereditary mixed polyposis syndrome | | | | 385 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | BMPR1A CL E G H | 657 | 1076 | ORPHA:157794 | Hereditary mixed polyposis syndrome | | | | 385 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BMPR1A CL E G H | 657 | 1076 | ORPHA:79076 | Juvenile polyposis of infancy | | | | 385 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BMPR1A CL E G H | 657 | 1076 | OMIM:174900 | Juvenile polyposis syndrome | | | | 385 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BMPR1A CL E G H | 657 | 1076 | OMIM:610069 | POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2 | | | | 385 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | BRAF CL E G H | 673 | 1097 | OMIM:114500 | Colorectal cancer | . | | | 276 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BRCA1 CL E G H | 672 | 1100 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 5769 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BRCA2 CL E G H | 675 | 1101 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 7642 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | BUB1 CL E G H | 699 | 1148 | OMIM:114500 | Colorectal cancer | . | | | 5 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BUB1 CL E G H | 699 | 1148 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | | | | 5 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | BUB1B CL E G H | 701 | 1149 | OMIM:114500 | Colorectal cancer | . | | | 76 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BUB1B CL E G H | 701 | 1149 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | | | | 76 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | BUB3 CL E G H | 9184 | 1151 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | | | | | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | CCND1 CL E G H | 595 | 1582 | OMIM:114500 | Colorectal cancer | . | | | 1 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 289 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:524 | Li-Fraumeni syndrome | | | | 289 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 289 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | CEP57 CL E G H | 9702 | 30794 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | | | | 17 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | CHEK2 CL E G H | 11200 | 16627 | OMIM:114500 | Colorectal cancer | . | | | 833 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | CHEK2 CL E G H | 11200 | 16627 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 833 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | CHEK2 CL E G H | 11200 | 16627 | ORPHA:524 | Li-Fraumeni syndrome | | | | 833 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | COL14A1 CL E G H | 7373 | 2191 | ORPHA:79501 | Punctate palmoplantar keratoderma type 1 | | | | 2 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | COL14A1 CL E G H | 7373 | 2191 | ORPHA:79501 | Punctate palmoplantar keratoderma type 1 | | | | 2 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | CTNNB1 CL E G H | 1499 | 2514 | OMIM:114500 | Colorectal cancer | . | | | 88 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | DCC CL E G H | 1630 | 2701 | OMIM:114500 | Colorectal cancer | . | | | 36 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | DICER1 CL E G H | 23405 | 17098 | ORPHA:276399 | Familial multinodular goiter | | | | 670 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | DLC1 CL E G H | 10395 | 2897 | OMIM:114500 | Colorectal cancer | . | | | 11 | | |
HP:0100834 | HP:0030437 | Anal canal neoplasm | 1 | DOCK8 CL E G H | 81704 | 19191 | ORPHA:217390 | Combined immunodeficiency due to DOCK8 deficiency | | | | 217 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | ENG CL E G H | 2022 | 3349 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | | | | 186 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | ENG CL E G H | 2022 | 3349 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | | | | 186 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | EP300 CL E G H | 2033 | 3373 | OMIM:114500 | Colorectal cancer | . | | | 250 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | EPCAM CL E G H | 4072 | 11529 | OMIM:613244 | Colorectal cancer, hereditary nonpolyposis, type 8 | | | | 170 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | EPCAM CL E G H | 4072 | 11529 | OMIM:613244 | Colorectal cancer, hereditary nonpolyposis, type 8 | . | | | 170 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | EPCAM CL E G H | 4072 | 11529 | ORPHA:144 | Lynch syndrome | | | | 170 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | EPCAM CL E G H | 4072 | 11529 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 170 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | FAN1 CL E G H | 22909 | 29170 | ORPHA:144 | Lynch syndrome | | | | 15 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | FAN1 CL E G H | 22909 | 29170 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 15 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | FGFR3 CL E G H | 2261 | 3690 | OMIM:114500 | Colorectal cancer | . | | | 145 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | FLCN CL E G H | 201163 | 27310 | OMIM:135150 | Birt-Hogg-Dube syndrome | | | | 332 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | FLCN CL E G H | 201163 | 27310 | OMIM:114500 | Colorectal cancer | . | | | 332 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | FOXE1 CL E G H | 2304 | 3806 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | | | | 9 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | GATA1 CL E G H | 2623 | 4170 | ORPHA:124 | Blackfan-Diamond anemia | | | | 29 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | GATA1 CL E G H | 2623 | 4170 | ORPHA:124 | Blackfan-Diamond anemia | | | | 29 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | GPR35 CL E G H | 2859 | 4492 | ORPHA:171 | Primary sclerosing cholangitis | HP:0040283 - Occasional | | | 2 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | GREM1 CL E G H | 26585 | 2001 | ORPHA:157794 | Hereditary mixed polyposis syndrome | | | | 9 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | GREM1 CL E G H | 26585 | 2001 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040283 - Occasional | | | 9 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | GREM1 CL E G H | 26585 | 2001 | ORPHA:157794 | Hereditary mixed polyposis syndrome | | | | 9 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | HABP2 CL E G H | 3026 | 4798 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | | | | 58 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | KEAP1 CL E G H | 9817 | 23177 | ORPHA:276399 | Familial multinodular goiter | | | | | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | KIT CL E G H | 3815 | 6342 | ORPHA:44890 | Gastrointestinal stromal tumor | HP:0040283 - Occasional | | | 327 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | KIT CL E G H | 3815 | 6342 | ORPHA:44890 | Gastrointestinal stromal tumor | HP:0040283 - Occasional | | | 327 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | KLLN CL E G H | 100144748 | 37212 | ORPHA:201 | Cowden syndrome | | | | 1 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | KRAS CL E G H | 3845 | 6407 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 196 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | KRAS CL E G H | 3845 | 6407 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 196 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | KRAS CL E G H | 3845 | 6407 | ORPHA:144 | Lynch syndrome | | | | 196 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MBD4 CL E G H | 8930 | 6919 | OMIM:619975 | | | | | 1 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | MCC CL E G H | 4163 | 6935 | OMIM:114500 | Colorectal cancer | . | | | 6 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MDM2 CL E G H | 4193 | 6973 | ORPHA:524 | Li-Fraumeni syndrome | | | | 1 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | MDM2 CL E G H | 4193 | 6973 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 1 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MINPP1 CL E G H | 9562 | 7102 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | | | | 3 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MLH1 CL E G H | 4292 | 7127 | OMIM:609310 | COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2; HNPCC2 | | | | 1819 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | MLH1 CL E G H | 4292 | 7127 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 1819 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MLH1 CL E G H | 4292 | 7127 | ORPHA:144 | Lynch syndrome | | | | 1819 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MLH1 CL E G H | 4292 | 7127 | OMIM:276300 | Mismatch repair cancer syndrome 1 | | | | 1819 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | MLH1 CL E G H | 4292 | 7127 | OMIM:276300 | Mismatch repair cancer syndrome 1 | | | | 1819 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MLH1 CL E G H | 4292 | 7127 | ORPHA:587 | Muir-Torre syndrome | | | | 1819 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MLH1 CL E G H | 4292 | 7127 | OMIM:158320 | Muir-Torre syndrome | | | | 1819 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | MLH3 CL E G H | 27030 | 7128 | OMIM:114500 | Colorectal cancer | . | | | 131 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | MLH3 CL E G H | 27030 | 7128 | OMIM:614385 | Colorectal cancer, hereditary nonpolyposis, type 7 | . | | | 131 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | MLH3 CL E G H | 27030 | 7128 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 131 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MLH3 CL E G H | 27030 | 7128 | ORPHA:144 | Lynch syndrome | | | | 131 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | MSH2 CL E G H | 4436 | 7325 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 2162 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MSH2 CL E G H | 4436 | 7325 | ORPHA:144 | Lynch syndrome | | | | 2162 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MSH2 CL E G H | 4436 | 7325 | OMIM:120435 | Lynch syndrome I | | | | 2162 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MSH2 CL E G H | 4436 | 7325 | OMIM:619096 | MISMATCH REPAIR CANCER SYNDROME 2; MMRCS2 | | | | 2162 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MSH2 CL E G H | 4436 | 7325 | OMIM:158320 | Muir-Torre syndrome | | | | 2162 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MSH2 CL E G H | 4436 | 7325 | ORPHA:587 | Muir-Torre syndrome | | | | 2162 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MSH3 CL E G H | 4437 | 7326 | OMIM:617100 | Familial adenomatous polyposis 4 | | | | 5 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | MSH3 CL E G H | 4437 | 7326 | ORPHA:480536 | MSH3-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 5 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MSH3 CL E G H | 4437 | 7326 | ORPHA:480536 | MSH3-related attenuated familial adenomatous polyposis | | | | 5 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | MSH6 CL E G H | 2956 | 7329 | OMIM:614350 | Colorectal cancer, hereditary nonpolyposis, type 5 | . | | | 2232 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | MSH6 CL E G H | 2956 | 7329 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 2232 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MSH6 CL E G H | 2956 | 7329 | ORPHA:144 | Lynch syndrome | | | | 2232 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MSH6 CL E G H | 2956 | 7329 | OMIM:619097 | MISMATCH REPAIR CANCER SYNDROME 3; MMRCS3 | | | | 2232 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | MSH6 CL E G H | 2956 | 7329 | OMIM:619097 | MISMATCH REPAIR CANCER SYNDROME 3; MMRCS3 | | | | 2232 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MSH6 CL E G H | 2956 | 7329 | ORPHA:587 | Muir-Torre syndrome | | | | 2232 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | MST1 CL E G H | 4485 | 7380 | ORPHA:171 | Primary sclerosing cholangitis | HP:0040283 - Occasional | | | 1 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MUTYH CL E G H | 4595 | 7527 | OMIM:608456 | Familial adenomatous polyposis, 2 | | | | 592 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | MUTYH CL E G H | 4595 | 7527 | ORPHA:247798 | MUTYH-related attenuated familial adenomatous polyposis | | | | 592 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | MUTYH CL E G H | 4595 | 7527 | ORPHA:247798 | MUTYH-related attenuated familial adenomatous polyposis | | | | 592 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | MUTYH CL E G H | 4595 | 7527 | ORPHA:247798 | MUTYH-related attenuated familial adenomatous polyposis | | | | 592 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | NRAS CL E G H | 4893 | 7989 | OMIM:114500 | Colorectal cancer | . | | | 102 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | NTHL1 CL E G H | 4913 | 8028 | OMIM:616415 | Familial adenomatous polyposis 3 | | | | 2 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | NTHL1 CL E G H | 4913 | 8028 | ORPHA:454840 | NTHL1-related attenuated familial adenomatous polyposis | | | | 2 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | NTHL1 CL E G H | 4913 | 8028 | ORPHA:454840 | NTHL1-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 2 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | PALB2 CL E G H | 79728 | 26144 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 1349 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | PALLD CL E G H | 23022 | 17068 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 192 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | PDE11A CL E G H | 50940 | 8773 | ORPHA:1359 | Carney complex | | | | 13 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | PDGFRA CL E G H | 5156 | 8803 | ORPHA:44890 | Gastrointestinal stromal tumor | HP:0040283 - Occasional | | | 337 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | PDGFRA CL E G H | 5156 | 8803 | ORPHA:44890 | Gastrointestinal stromal tumor | HP:0040283 - Occasional | | | 337 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | PDGFRL CL E G H | 5157 | 8805 | OMIM:114500 | Colorectal cancer | . | | | 2 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | PIK3CA CL E G H | 5290 | 8975 | OMIM:114500 | Colorectal cancer | . | | | 162 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:201 | Cowden syndrome | | | | 162 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 162 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:144 | Lynch syndrome | | | | 162 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | PLA2G2A CL E G H | 5320 | 9031 | OMIM:114500 | Colorectal cancer | . | | | 1 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | PMS1 CL E G H | 5378 | 9121 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 56 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | PMS1 CL E G H | 5378 | 9121 | ORPHA:144 | Lynch syndrome | | | | 56 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | PMS1 CL E G H | 5378 | 9121 | OMIM:120435 | Lynch syndrome I | | | | 56 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | PMS2 CL E G H | 5395 | 9122 | OMIM:614337 | Colorectal cancer, hereditary nonpolyposis, type 4 | . | | | 1121 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | PMS2 CL E G H | 5395 | 9122 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 1121 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | PMS2 CL E G H | 5395 | 9122 | ORPHA:144 | Lynch syndrome | | | | 1121 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | PMS2 CL E G H | 5395 | 9122 | OMIM:619101 | MISMATCH REPAIR CANCER SYNDROME 4; MMRCS4 | | | | 1121 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | POLD1 CL E G H | 5424 | 9175 | OMIM:612591 | Colorectal cancer, susceptibility to, 10 | | | | 731 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | POLD1 CL E G H | 5424 | 9175 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | | | | 731 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | POLD1 CL E G H | 5424 | 9175 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | HP:0040283 - Occasional | | | 731 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | POLD1 CL E G H | 5424 | 9175 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | | | | 731 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | POLE CL E G H | 5426 | 9177 | OMIM:615083 | Colorectal cancer, susceptibility to, 12 | | | | 1129 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | POLE CL E G H | 5426 | 9177 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | HP:0040283 - Occasional | | | 1129 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | POLE CL E G H | 5426 | 9177 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | | | | 1129 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | POLE CL E G H | 5426 | 9177 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | | | | 1129 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | PRKAR1A CL E G H | 5573 | 9388 | ORPHA:1359 | Carney complex | | | | 134 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | PTEN CL E G H | 5728 | 9588 | ORPHA:201 | Cowden syndrome | | | | 948 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | PTEN CL E G H | 5728 | 9588 | ORPHA:79076 | Juvenile polyposis of infancy | | | | 948 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | PTPN12 CL E G H | 5782 | 9645 | OMIM:114500 | Colorectal cancer | . | | | 1 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | PTPRJ CL E G H | 5795 | 9673 | OMIM:114500 | Colorectal cancer | . | | | 3 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RABL3 CL E G H | 285282 | 18072 | ORPHA:1333 | Familial pancreatic carcinoma | | | | | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | RAD54B CL E G H | 25788 | 17228 | OMIM:114500 | Colorectal cancer | . | | | 2 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RNF43 CL E G H | 54894 | 18505 | ORPHA:157798 | Serrated polyposis syndrome | | | | 5 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | RNF43 CL E G H | 54894 | 18505 | ORPHA:157798 | Serrated polyposis syndrome | | | | 5 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPL11 CL E G H | 6135 | 10301 | ORPHA:124 | Blackfan-Diamond anemia | | | | 22 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPL11 CL E G H | 6135 | 10301 | ORPHA:124 | Blackfan-Diamond anemia | | | | 22 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPL15 CL E G H | 6138 | 10306 | ORPHA:124 | Blackfan-Diamond anemia | | | | 3 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPL15 CL E G H | 6138 | 10306 | ORPHA:124 | Blackfan-Diamond anemia | | | | 3 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPL18 CL E G H | 6141 | 10310 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPL18 CL E G H | 6141 | 10310 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPL26 CL E G H | 6154 | 10327 | ORPHA:124 | Blackfan-Diamond anemia | | | | 3 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPL26 CL E G H | 6154 | 10327 | ORPHA:124 | Blackfan-Diamond anemia | | | | 3 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPL27 CL E G H | 6155 | 10328 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPL27 CL E G H | 6155 | 10328 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPL31 CL E G H | 6160 | 10334 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPL31 CL E G H | 6160 | 10334 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPL35 CL E G H | 11224 | 10344 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPL35 CL E G H | 11224 | 10344 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPL35A CL E G H | 6165 | 10345 | ORPHA:124 | Blackfan-Diamond anemia | | | | 11 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPL35A CL E G H | 6165 | 10345 | ORPHA:124 | Blackfan-Diamond anemia | | | | 11 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPL5 CL E G H | 6125 | 10360 | ORPHA:124 | Blackfan-Diamond anemia | | | | 40 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPL5 CL E G H | 6125 | 10360 | ORPHA:124 | Blackfan-Diamond anemia | | | | 40 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS10 CL E G H | 6204 | 10383 | ORPHA:124 | Blackfan-Diamond anemia | | | | 26 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS10 CL E G H | 6204 | 10383 | ORPHA:124 | Blackfan-Diamond anemia | | | | 26 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS15A CL E G H | 6210 | 10389 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS15A CL E G H | 6210 | 10389 | ORPHA:124 | Blackfan-Diamond anemia | | | | | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS17 CL E G H | 6218 | 10397 | ORPHA:124 | Blackfan-Diamond anemia | | | | 5 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS17 CL E G H | 6218 | 10397 | ORPHA:124 | Blackfan-Diamond anemia | | | | 5 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS19 CL E G H | 6223 | 10402 | ORPHA:124 | Blackfan-Diamond anemia | | | | 42 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS19 CL E G H | 6223 | 10402 | ORPHA:124 | Blackfan-Diamond anemia | | | | 42 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS19 CL E G H | 6223 | 10402 | OMIM:105650 | Diamond-Blackfan anemia 1 | | | | 42 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS20 CL E G H | 6224 | 10405 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS20 CL E G H | 6224 | 10405 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS20 CL E G H | 6224 | 10405 | ORPHA:440437 | Familial colorectal cancer Type X | HP:0040283 - Occasional | | | 1 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | RPS20 CL E G H | 6224 | 10405 | ORPHA:440437 | Familial colorectal cancer Type X | HP:0040282 - Frequent | | | 1 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS24 CL E G H | 6229 | 10411 | ORPHA:124 | Blackfan-Diamond anemia | | | | 22 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS24 CL E G H | 6229 | 10411 | ORPHA:124 | Blackfan-Diamond anemia | | | | 22 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS26 CL E G H | 6231 | 10414 | ORPHA:124 | Blackfan-Diamond anemia | | | | 20 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS26 CL E G H | 6231 | 10414 | ORPHA:124 | Blackfan-Diamond anemia | | | | 20 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS27 CL E G H | 6232 | 10416 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS27 CL E G H | 6232 | 10416 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS28 CL E G H | 6234 | 10418 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS28 CL E G H | 6234 | 10418 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS29 CL E G H | 6235 | 10419 | ORPHA:124 | Blackfan-Diamond anemia | | | | 3 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS29 CL E G H | 6235 | 10419 | ORPHA:124 | Blackfan-Diamond anemia | | | | 3 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | RPS7 CL E G H | 6201 | 10440 | ORPHA:124 | Blackfan-Diamond anemia | | | | 20 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | RPS7 CL E G H | 6201 | 10440 | ORPHA:124 | Blackfan-Diamond anemia | | | | 20 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | SDHA CL E G H | 6389 | 10680 | ORPHA:44890 | Gastrointestinal stromal tumor | HP:0040283 - Occasional | | | 304 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | SDHA CL E G H | 6389 | 10680 | ORPHA:44890 | Gastrointestinal stromal tumor | HP:0040283 - Occasional | | | 304 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | SDHB CL E G H | 6390 | 10681 | ORPHA:201 | Cowden syndrome | | | | 237 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | SDHB CL E G H | 6390 | 10681 | ORPHA:44890 | Gastrointestinal stromal tumor | HP:0040283 - Occasional | | | 237 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | SDHB CL E G H | 6390 | 10681 | ORPHA:44890 | Gastrointestinal stromal tumor | HP:0040283 - Occasional | | | 237 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | SDHC CL E G H | 6391 | 10682 | ORPHA:201 | Cowden syndrome | | | | 147 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | SDHC CL E G H | 6391 | 10682 | ORPHA:44890 | Gastrointestinal stromal tumor | HP:0040283 - Occasional | | | 147 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | SDHC CL E G H | 6391 | 10682 | ORPHA:44890 | Gastrointestinal stromal tumor | HP:0040283 - Occasional | | | 147 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | SDHD CL E G H | 6392 | 10683 | ORPHA:201 | Cowden syndrome | | | | 129 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | SEC23B CL E G H | 10483 | 10702 | ORPHA:201 | Cowden syndrome | | | | 60 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | SEMA4A CL E G H | 64218 | 10729 | ORPHA:440437 | Familial colorectal cancer Type X | HP:0040283 - Occasional | | | 48 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | SEMA4A CL E G H | 64218 | 10729 | ORPHA:440437 | Familial colorectal cancer Type X | HP:0040282 - Frequent | | | 48 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | SEMA4D CL E G H | 10507 | 10732 | ORPHA:171 | Primary sclerosing cholangitis | HP:0040283 - Occasional | | | | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | SH3KBP1 CL E G H | 30011 | 13867 | OMIM:300310 | Immunodeficiency 61 | | | | 2 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | SMAD4 CL E G H | 4089 | 6770 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 504 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | SMAD4 CL E G H | 4089 | 6770 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | | | | 504 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | SMAD4 CL E G H | 4089 | 6770 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | | | | 504 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | SMAD4 CL E G H | 4089 | 6770 | OMIM:174900 | Juvenile polyposis syndrome | | | | 504 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | SMAD7 CL E G H | 4092 | 6773 | OMIM:612229 | Caudal duplication anomaly | | | | 1 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | SRC CL E G H | 6714 | 11283 | OMIM:114500 | Colorectal cancer | . | | | 15 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | STK11 CL E G H | 6794 | 11389 | ORPHA:2869 | Peutz-Jeghers syndrome | HP:0040283 - Occasional | | | 740 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | STK11 CL E G H | 6794 | 11389 | ORPHA:2869 | Peutz-Jeghers syndrome | HP:0040283 - Occasional | | | 740 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | TCF4 CL E G H | 6925 | 11634 | ORPHA:171 | Primary sclerosing cholangitis | HP:0040283 - Occasional | | | 241 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | TGFBR2 CL E G H | 7048 | 11773 | OMIM:614331 | COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6; HNPCC6 | | | | 253 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | TGFBR2 CL E G H | 7048 | 11773 | ORPHA:144 | Lynch syndrome | HP:0040282 - Frequent | | | 253 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | TGFBR2 CL E G H | 7048 | 11773 | ORPHA:144 | Lynch syndrome | | | | 253 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | TLR2 CL E G H | 7097 | 11848 | OMIM:114500 | Colorectal cancer | . | | | 5 | | |
HP:0100834 | HP:0006716 | Hereditary nonpolyposis colorectal carcinoma | 1 | TP53 CL E G H | 7157 | 11998 | OMIM:114500 | Colorectal cancer | . | | | 911 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | TP53 CL E G H | 7157 | 11998 | ORPHA:1333 | Familial pancreatic carcinoma | | | | 911 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | TP53 CL E G H | 7157 | 11998 | OMIM:151623 | Li-Fraumeni syndrome | | | | 911 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | TP53 CL E G H | 7157 | 11998 | ORPHA:524 | Li-Fraumeni syndrome | | | | 911 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | TP53 CL E G H | 7157 | 11998 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 911 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | TRIP13 CL E G H | 9319 | 12307 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | | | | 2 | | |
HP:0100834 | HP:0100273 | Neoplasm of the colon | 1 | TSR2 CL E G H | 90121 | 25455 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0040275 | Adenocarcinoma of the large intestine | 1 | TSR2 CL E G H | 90121 | 25455 | ORPHA:124 | Blackfan-Diamond anemia | | | | 1 | | |
HP:0100834 | HP:0100743 | Neoplasm of the rectum | 1 | USF3 CL E G H | 205717 | 30494 | ORPHA:201 | Cowden syndrome | | | | 1 | | |
HP:0100834 | HP:0030439 | Anal canal adenocarcinoma | 2 | CL E G H | | | | | | | | | | |
HP:0100834 | HP:0030438 | Anal canal squamous cell carcinoma | 2 | CL E G H | | | | | | | | | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | AAGAB CL E G H | 79719 | 25662 | ORPHA:79501 | Punctate palmoplantar keratoderma type 1 | HP:0040284 - Very rare | | | 7 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | ADA2 CL E G H | 51816 | 1839 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 22 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | AKT1 CL E G H | 207 | 391 | ORPHA:201 | Cowden syndrome | HP:0040281 - Very frequent | | | 54 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | APC CL E G H | 324 | 583 | OMIM:175100 | Adenomatous polyposis coli | | | | 3179 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | APC CL E G H | 324 | 583 | OMIM:175100 | Adenomatous polyposis coli | | | | 3179 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | APC CL E G H | 324 | 583 | ORPHA:247806 | APC-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 3179 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | APC CL E G H | 324 | 583 | ORPHA:247806 | APC-related attenuated familial adenomatous polyposis | HP:0040281 - Very frequent | | | 3179 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | APC CL E G H | 324 | 583 | OMIM:135290 | Desmoid disease, hereditary | | | | 3179 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | APC CL E G H | 324 | 583 | OMIM:135290 | Desmoid disease, hereditary | | | | 3179 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | APC CL E G H | 324 | 583 | ORPHA:261584 | Familial adenomatous polyposis due to 5q22.2 microdeletion | HP:0040283 - Occasional | | | 3179 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | APC CL E G H | 324 | 583 | ORPHA:261584 | Familial adenomatous polyposis due to 5q22.2 microdeletion | HP:0040281 - Very frequent | | | 3179 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | APC CL E G H | 324 | 583 | ORPHA:79665 | Gardner syndrome | HP:0040282 - Frequent | | | 3179 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | APC CL E G H | 324 | 583 | ORPHA:79665 | Gardner syndrome | HP:0040281 - Very frequent | | | 3179 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | APC CL E G H | 324 | 583 | ORPHA:99818 | Turcot syndrome with polyposis | HP:0040281 - Very frequent | | | 3179 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | APC CL E G H | 324 | 583 | ORPHA:99818 | Turcot syndrome with polyposis | HP:0040281 - Very frequent | | | 3179 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | AXIN2 CL E G H | 8313 | 904 | ORPHA:401911 | AXIN2-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 435 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | AXIN2 CL E G H | 8313 | 904 | ORPHA:401911 | AXIN2-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 435 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | AXIN2 CL E G H | 8313 | 904 | ORPHA:401911 | AXIN2-related attenuated familial adenomatous polyposis | HP:0040283 - Occasional | | | 435 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | AXIN2 CL E G H | 8313 | 904 | OMIM:608615 | OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS | | | | 435 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | AXIN2 CL E G H | 8313 | 904 | OMIM:608615 | OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS | | | | 435 | | |
HP:0100834 | HP:0100896 | Rectal polyposis | 2 | BMPR1A CL E G H | 657 | 1076 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | HP:0040282 - Frequent | | | 385 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | BMPR1A CL E G H | 657 | 1076 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | HP:0040282 - Frequent | | | 385 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | BMPR1A CL E G H | 657 | 1076 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040282 - Frequent | | | 385 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | BMPR1A CL E G H | 657 | 1076 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040283 - Occasional | | | 385 | | |
HP:0100834 | HP:0100896 | Rectal polyposis | 2 | BMPR1A CL E G H | 657 | 1076 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040282 - Frequent | | | 385 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | BMPR1A CL E G H | 657 | 1076 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040282 - Frequent | | | 385 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | BMPR1A CL E G H | 657 | 1076 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040282 - Frequent | | | 385 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | BMPR1A CL E G H | 657 | 1076 | ORPHA:79076 | Juvenile polyposis of infancy | HP:0040280 - Obligate | | | 385 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | BMPR1A CL E G H | 657 | 1076 | OMIM:174900 | Juvenile polyposis syndrome | | | | 385 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | BMPR1A CL E G H | 657 | 1076 | OMIM:610069 | POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2 | | | | 385 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | BMPR1A CL E G H | 657 | 1076 | OMIM:610069 | POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2 | | | | 385 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | BRCA1 CL E G H | 672 | 1100 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 5769 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | BRCA2 CL E G H | 675 | 1101 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 7642 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | BUB1 CL E G H | 699 | 1148 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 5 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | BUB1B CL E G H | 701 | 1149 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 76 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | BUB3 CL E G H | 9184 | 1151 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 289 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040283 - Occasional | | | 289 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 289 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | CEP57 CL E G H | 9702 | 30794 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 17 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | CHEK2 CL E G H | 11200 | 16627 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040283 - Occasional | | | 833 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | CHEK2 CL E G H | 11200 | 16627 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 833 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | COL14A1 CL E G H | 7373 | 2191 | ORPHA:79501 | Punctate palmoplantar keratoderma type 1 | HP:0040284 - Very rare | | | 2 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | DICER1 CL E G H | 23405 | 17098 | ORPHA:276399 | Familial multinodular goiter | HP:0040282 - Frequent | | | 670 | | |
HP:0100834 | HP:0006763 | Anal canal squamous carcinoma | 2 | DOCK8 CL E G H | 81704 | 19191 | ORPHA:217390 | Combined immunodeficiency due to DOCK8 deficiency | HP:0040283 - Occasional | | | 217 | | |
HP:0100834 | HP:0100896 | Rectal polyposis | 2 | ENG CL E G H | 2022 | 3349 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | HP:0040282 - Frequent | | | 186 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | ENG CL E G H | 2022 | 3349 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | HP:0040282 - Frequent | | | 186 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | EPCAM CL E G H | 4072 | 11529 | OMIM:613244 | Colorectal cancer, hereditary nonpolyposis, type 8 | | | | 170 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | EPCAM CL E G H | 4072 | 11529 | OMIM:613244 | Colorectal cancer, hereditary nonpolyposis, type 8 | | | | 170 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | EPCAM CL E G H | 4072 | 11529 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 170 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | FAN1 CL E G H | 22909 | 29170 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 15 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | FLCN CL E G H | 201163 | 27310 | OMIM:135150 | Birt-Hogg-Dube syndrome | | | | 332 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | FOXE1 CL E G H | 2304 | 3806 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040283 - Occasional | | | 9 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | GATA1 CL E G H | 2623 | 4170 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 29 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | GREM1 CL E G H | 26585 | 2001 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040282 - Frequent | | | 9 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | GREM1 CL E G H | 26585 | 2001 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040282 - Frequent | | | 9 | | |
HP:0100834 | HP:0100896 | Rectal polyposis | 2 | GREM1 CL E G H | 26585 | 2001 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040282 - Frequent | | | 9 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | GREM1 CL E G H | 26585 | 2001 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040282 - Frequent | | | 9 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | GREM1 CL E G H | 26585 | 2001 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040283 - Occasional | | | 9 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | HABP2 CL E G H | 3026 | 4798 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040283 - Occasional | | | 58 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | KEAP1 CL E G H | 9817 | 23177 | ORPHA:276399 | Familial multinodular goiter | HP:0040282 - Frequent | | | | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | KLLN CL E G H | 100144748 | 37212 | ORPHA:201 | Cowden syndrome | HP:0040281 - Very frequent | | | 1 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | KRAS CL E G H | 3845 | 6407 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 196 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | KRAS CL E G H | 3845 | 6407 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 196 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | MBD4 CL E G H | 8930 | 6919 | OMIM:619975 | | | | | 1 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MBD4 CL E G H | 8930 | 6919 | OMIM:619975 | | | | | 1 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MDM2 CL E G H | 4193 | 6973 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 1 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | MDM2 CL E G H | 4193 | 6973 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MINPP1 CL E G H | 9562 | 7102 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040283 - Occasional | | | 3 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MLH1 CL E G H | 4292 | 7127 | OMIM:609310 | COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2; HNPCC2 | | | | 1819 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MLH1 CL E G H | 4292 | 7127 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 1819 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | MLH1 CL E G H | 4292 | 7127 | OMIM:276300 | Mismatch repair cancer syndrome 1 | | | | 1819 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | MLH1 CL E G H | 4292 | 7127 | OMIM:276300 | Mismatch repair cancer syndrome 1 | | | | 1819 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MLH1 CL E G H | 4292 | 7127 | OMIM:158320 | Muir-Torre syndrome | . | | | 1819 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MLH1 CL E G H | 4292 | 7127 | ORPHA:587 | Muir-Torre syndrome | HP:0040282 - Frequent | | | 1819 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MLH3 CL E G H | 27030 | 7128 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 131 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MSH2 CL E G H | 4436 | 7325 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 2162 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MSH2 CL E G H | 4436 | 7325 | OMIM:120435 | Lynch syndrome I | . | | | 2162 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MSH2 CL E G H | 4436 | 7325 | OMIM:619096 | MISMATCH REPAIR CANCER SYNDROME 2; MMRCS2 | | | | 2162 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MSH2 CL E G H | 4436 | 7325 | ORPHA:587 | Muir-Torre syndrome | HP:0040282 - Frequent | | | 2162 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MSH2 CL E G H | 4436 | 7325 | OMIM:158320 | Muir-Torre syndrome | . | | | 2162 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | MSH3 CL E G H | 4437 | 7326 | OMIM:617100 | Familial adenomatous polyposis 4 | | | | 5 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MSH3 CL E G H | 4437 | 7326 | ORPHA:480536 | MSH3-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 5 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | MSH3 CL E G H | 4437 | 7326 | ORPHA:480536 | MSH3-related attenuated familial adenomatous polyposis | HP:0040281 - Very frequent | | | 5 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | MSH3 CL E G H | 4437 | 7326 | ORPHA:480536 | MSH3-related attenuated familial adenomatous polyposis | HP:0040281 - Very frequent | | | 5 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MSH6 CL E G H | 2956 | 7329 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 2232 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MSH6 CL E G H | 2956 | 7329 | OMIM:619097 | MISMATCH REPAIR CANCER SYNDROME 3; MMRCS3 | | | | 2232 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MSH6 CL E G H | 2956 | 7329 | ORPHA:587 | Muir-Torre syndrome | HP:0040282 - Frequent | | | 2232 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | MUTYH CL E G H | 4595 | 7527 | OMIM:608456 | Familial adenomatous polyposis, 2 | | | | 592 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | MUTYH CL E G H | 4595 | 7527 | OMIM:608456 | Familial adenomatous polyposis, 2 | . | | | 592 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | MUTYH CL E G H | 4595 | 7527 | ORPHA:247798 | MUTYH-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 592 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | MUTYH CL E G H | 4595 | 7527 | ORPHA:247798 | MUTYH-related attenuated familial adenomatous polyposis | HP:0040281 - Very frequent | | | 592 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | MUTYH CL E G H | 4595 | 7527 | ORPHA:247798 | MUTYH-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 592 | | |
HP:0100834 | HP:0100896 | Rectal polyposis | 2 | MUTYH CL E G H | 4595 | 7527 | ORPHA:247798 | MUTYH-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 592 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | NTHL1 CL E G H | 4913 | 8028 | OMIM:616415 | Familial adenomatous polyposis 3 | | | | 2 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | NTHL1 CL E G H | 4913 | 8028 | OMIM:616415 | Familial adenomatous polyposis 3 | | | | 2 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | NTHL1 CL E G H | 4913 | 8028 | ORPHA:454840 | NTHL1-related attenuated familial adenomatous polyposis | HP:0040281 - Very frequent | | | 2 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | NTHL1 CL E G H | 4913 | 8028 | ORPHA:454840 | NTHL1-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 2 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | PALB2 CL E G H | 79728 | 26144 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 1349 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | PALLD CL E G H | 23022 | 17068 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 192 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:201 | Cowden syndrome | HP:0040281 - Very frequent | | | 162 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 162 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | PMS1 CL E G H | 5378 | 9121 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 56 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | PMS1 CL E G H | 5378 | 9121 | OMIM:120435 | Lynch syndrome I | . | | | 56 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | PMS2 CL E G H | 5395 | 9122 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 1121 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | PMS2 CL E G H | 5395 | 9122 | OMIM:619101 | MISMATCH REPAIR CANCER SYNDROME 4; MMRCS4 | | | | 1121 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | PMS2 CL E G H | 5395 | 9122 | OMIM:619101 | MISMATCH REPAIR CANCER SYNDROME 4; MMRCS4 | | | | 1121 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | POLD1 CL E G H | 5424 | 9175 | OMIM:612591 | Colorectal cancer, susceptibility to, 10 | . | | | 731 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | POLD1 CL E G H | 5424 | 9175 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | HP:0040283 - Occasional | | | 731 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | POLD1 CL E G H | 5424 | 9175 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | HP:0040282 - Frequent | | | 731 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | POLD1 CL E G H | 5424 | 9175 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | HP:0040282 - Frequent | | | 731 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | POLE CL E G H | 5426 | 9177 | OMIM:615083 | Colorectal cancer, susceptibility to, 12 | . | | | 1129 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | POLE CL E G H | 5426 | 9177 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | HP:0040283 - Occasional | | | 1129 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | POLE CL E G H | 5426 | 9177 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | HP:0040282 - Frequent | | | 1129 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | POLE CL E G H | 5426 | 9177 | ORPHA:447877 | Polymerase proofreading-related adenomatous polyposis | HP:0040282 - Frequent | | | 1129 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | PTEN CL E G H | 5728 | 9588 | ORPHA:201 | Cowden syndrome | HP:0040281 - Very frequent | | | 948 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | PTEN CL E G H | 5728 | 9588 | ORPHA:79076 | Juvenile polyposis of infancy | HP:0040280 - Obligate | | | 948 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | RABL3 CL E G H | 285282 | 18072 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | RNF43 CL E G H | 54894 | 18505 | ORPHA:157798 | Serrated polyposis syndrome | HP:0040281 - Very frequent | | | 5 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | RNF43 CL E G H | 54894 | 18505 | ORPHA:157798 | Serrated polyposis syndrome | HP:0040282 - Frequent | | | 5 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPL11 CL E G H | 6135 | 10301 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 22 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPL15 CL E G H | 6138 | 10306 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 3 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPL18 CL E G H | 6141 | 10310 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPL26 CL E G H | 6154 | 10327 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 3 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPL27 CL E G H | 6155 | 10328 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 1 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPL31 CL E G H | 6160 | 10334 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPL35 CL E G H | 11224 | 10344 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPL35A CL E G H | 6165 | 10345 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 11 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPL5 CL E G H | 6125 | 10360 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 40 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS10 CL E G H | 6204 | 10383 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 26 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS15A CL E G H | 6210 | 10389 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS17 CL E G H | 6218 | 10397 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 5 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS19 CL E G H | 6223 | 10402 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 42 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | RPS19 CL E G H | 6223 | 10402 | OMIM:105650 | Diamond-Blackfan anemia 1 | . | | | 42 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS20 CL E G H | 6224 | 10405 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 1 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS24 CL E G H | 6229 | 10411 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 22 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS26 CL E G H | 6231 | 10414 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 20 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS27 CL E G H | 6232 | 10416 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 1 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS28 CL E G H | 6234 | 10418 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 1 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS29 CL E G H | 6235 | 10419 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 3 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | RPS7 CL E G H | 6201 | 10440 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 20 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | SDHB CL E G H | 6390 | 10681 | ORPHA:201 | Cowden syndrome | HP:0040281 - Very frequent | | | 237 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | SDHC CL E G H | 6391 | 10682 | ORPHA:201 | Cowden syndrome | HP:0040281 - Very frequent | | | 147 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | SDHD CL E G H | 6392 | 10683 | ORPHA:201 | Cowden syndrome | HP:0040281 - Very frequent | | | 129 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | SEC23B CL E G H | 10483 | 10702 | ORPHA:201 | Cowden syndrome | HP:0040281 - Very frequent | | | 60 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | SH3KBP1 CL E G H | 30011 | 13867 | OMIM:300310 | Immunodeficiency 61 | . | | | 2 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | SMAD4 CL E G H | 4089 | 6770 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 504 | | |
HP:0100834 | HP:0005227 | Adenomatous colonic polyposis | 2 | SMAD4 CL E G H | 4089 | 6770 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | HP:0040282 - Frequent | | | 504 | | |
HP:0100834 | HP:0100896 | Rectal polyposis | 2 | SMAD4 CL E G H | 4089 | 6770 | ORPHA:329971 | Generalized juvenile polyposis/juvenile polyposis coli | HP:0040282 - Frequent | | | 504 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | SMAD4 CL E G H | 4089 | 6770 | OMIM:174900 | Juvenile polyposis syndrome | | | | 504 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | SMAD7 CL E G H | 4092 | 6773 | OMIM:612229 | Caudal duplication anomaly | | | | 1 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | TGFBR2 CL E G H | 7048 | 11773 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 253 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | TP53 CL E G H | 7157 | 11998 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 911 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | TP53 CL E G H | 7157 | 11998 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 911 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | TP53 CL E G H | 7157 | 11998 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040283 - Occasional | | | 911 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | TP53 CL E G H | 7157 | 11998 | OMIM:151623 | Li-Fraumeni syndrome | . | | | 911 | | |
HP:0100834 | HP:0003003 | Colon cancer | 2 | TRIP13 CL E G H | 9319 | 12307 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 2 | | |
HP:0100834 | HP:0040276 | Adenocarcinoma of the colon | 2 | TSR2 CL E G H | 90121 | 25455 | ORPHA:124 | Blackfan-Diamond anemia | HP:0040284 - Very rare | | | 1 | | |
HP:0100834 | HP:0200063 | Colorectal polyposis | 2 | USF3 CL E G H | 205717 | 30494 | ORPHA:201 | Cowden syndrome | HP:0040281 - Very frequent | | | 1 | | |