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:0003003 | HP:0003003 | Colon cancer | 0 | APC CL E G H | 324 | 583 | OMIM:175100 | Adenomatous polyposis coli | | | | 3179 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | APC CL E G H | 324 | 583 | ORPHA:247806 | APC-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 3179 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | APC CL E G H | 324 | 583 | OMIM:135290 | Desmoid disease, hereditary | | | | 3179 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | APC CL E G H | 324 | 583 | ORPHA:261584 | Familial adenomatous polyposis due to 5q22.2 microdeletion | HP:0040283 - Occasional | | | 3179 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | APC CL E G H | 324 | 583 | ORPHA:79665 | Gardner syndrome | HP:0040282 - Frequent | | | 3179 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | APC CL E G H | 324 | 583 | ORPHA:99818 | Turcot syndrome with polyposis | HP:0040281 - Very frequent | | | 3179 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | AXIN2 CL E G H | 8313 | 904 | ORPHA:401911 | AXIN2-related attenuated familial adenomatous polyposis | HP:0040283 - Occasional | | | 435 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | AXIN2 CL E G H | 8313 | 904 | OMIM:608615 | OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS | | | | 435 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | BMPR1A CL E G H | 657 | 1076 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040282 - Frequent | | | 385 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | BMPR1A CL E G H | 657 | 1076 | OMIM:174900 | Juvenile polyposis syndrome | | | | 385 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | BMPR1A CL E G H | 657 | 1076 | OMIM:610069 | POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2 | | | | 385 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | BRCA1 CL E G H | 672 | 1100 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 5769 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | BRCA2 CL E G H | 675 | 1101 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 7642 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | BUB1 CL E G H | 699 | 1148 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 5 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | BUB1B CL E G H | 701 | 1149 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 76 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | BUB3 CL E G H | 9184 | 1151 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 289 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 289 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | CEP57 CL E G H | 9702 | 30794 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 17 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | CHEK2 CL E G H | 11200 | 16627 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 833 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | EPCAM CL E G H | 4072 | 11529 | OMIM:613244 | Colorectal cancer, hereditary nonpolyposis, type 8 | | | | 170 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | EPCAM CL E G H | 4072 | 11529 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 170 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | FAN1 CL E G H | 22909 | 29170 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 15 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | FLCN CL E G H | 201163 | 27310 | OMIM:135150 | Birt-Hogg-Dube syndrome | | | | 332 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | FOXE1 CL E G H | 2304 | 3806 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040283 - Occasional | | | 9 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | GREM1 CL E G H | 26585 | 2001 | ORPHA:157794 | Hereditary mixed polyposis syndrome | HP:0040282 - Frequent | | | 9 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | HABP2 CL E G H | 3026 | 4798 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040283 - Occasional | | | 58 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | KRAS CL E G H | 3845 | 6407 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 196 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | KRAS CL E G H | 3845 | 6407 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 196 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MBD4 CL E G H | 8930 | 6919 | OMIM:619975 | | | | | 1 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MDM2 CL E G H | 4193 | 6973 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 1 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MINPP1 CL E G H | 9562 | 7102 | ORPHA:319487 | Familial papillary or follicular thyroid carcinoma | HP:0040283 - Occasional | | | 3 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MLH1 CL E G H | 4292 | 7127 | OMIM:609310 | COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2; HNPCC2 | | | | 1819 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MLH1 CL E G H | 4292 | 7127 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 1819 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MLH1 CL E G H | 4292 | 7127 | OMIM:158320 | Muir-Torre syndrome | . | | | 1819 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MLH1 CL E G H | 4292 | 7127 | ORPHA:587 | Muir-Torre syndrome | HP:0040282 - Frequent | | | 1819 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MLH3 CL E G H | 27030 | 7128 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 131 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MSH2 CL E G H | 4436 | 7325 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 2162 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MSH2 CL E G H | 4436 | 7325 | OMIM:120435 | Lynch syndrome I | . | | | 2162 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MSH2 CL E G H | 4436 | 7325 | OMIM:619096 | MISMATCH REPAIR CANCER SYNDROME 2; MMRCS2 | | | | 2162 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MSH2 CL E G H | 4436 | 7325 | OMIM:158320 | Muir-Torre syndrome | . | | | 2162 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MSH2 CL E G H | 4436 | 7325 | ORPHA:587 | Muir-Torre syndrome | HP:0040282 - Frequent | | | 2162 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MSH3 CL E G H | 4437 | 7326 | ORPHA:480536 | MSH3-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 5 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MSH6 CL E G H | 2956 | 7329 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 2232 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MSH6 CL E G H | 2956 | 7329 | OMIM:619097 | MISMATCH REPAIR CANCER SYNDROME 3; MMRCS3 | | | | 2232 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MSH6 CL E G H | 2956 | 7329 | ORPHA:587 | Muir-Torre syndrome | HP:0040282 - Frequent | | | 2232 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | MUTYH CL E G H | 4595 | 7527 | OMIM:608456 | Familial adenomatous polyposis, 2 | | | | 592 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | NTHL1 CL E G H | 4913 | 8028 | OMIM:616415 | Familial adenomatous polyposis 3 | | | | 2 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | NTHL1 CL E G H | 4913 | 8028 | ORPHA:454840 | NTHL1-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 2 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | PALB2 CL E G H | 79728 | 26144 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 1349 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | PALLD CL E G H | 23022 | 17068 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 192 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 162 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | PMS1 CL E G H | 5378 | 9121 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 56 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | PMS1 CL E G H | 5378 | 9121 | OMIM:120435 | Lynch syndrome I | . | | | 56 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | PMS2 CL E G H | 5395 | 9122 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 1121 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | PMS2 CL E G H | 5395 | 9122 | OMIM:619101 | MISMATCH REPAIR CANCER SYNDROME 4; MMRCS4 | | | | 1121 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | RABL3 CL E G H | 285282 | 18072 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | RPS19 CL E G H | 6223 | 10402 | OMIM:105650 | Diamond-Blackfan anemia 1 | . | | | 42 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | SH3KBP1 CL E G H | 30011 | 13867 | OMIM:300310 | Immunodeficiency 61 | . | | | 2 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | SMAD4 CL E G H | 4089 | 6770 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 504 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | SMAD4 CL E G H | 4089 | 6770 | OMIM:174900 | Juvenile polyposis syndrome | | | | 504 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | SMAD7 CL E G H | 4092 | 6773 | OMIM:612229 | Caudal duplication anomaly | | | | 1 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | TGFBR2 CL E G H | 7048 | 11773 | ORPHA:144 | Lynch syndrome | HP:0040281 - Very frequent | | | 253 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | TP53 CL E G H | 7157 | 11998 | ORPHA:1333 | Familial pancreatic carcinoma | HP:0040283 - Occasional | | | 911 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | TP53 CL E G H | 7157 | 11998 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040284 - Very rare | | | 911 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | TP53 CL E G H | 7157 | 11998 | OMIM:151623 | Li-Fraumeni syndrome | . | | | 911 | | |
HP:0003003 | HP:0003003 | Colon cancer | 0 | TRIP13 CL E G H | 9319 | 12307 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 2 | | |