Term ID: |
12126 |
Name: |
Stomach cancer |
Synonym: |
Gastric cancer |
Definition: |
A cancer arising in any part of the stomach. |
Comments: |
|
Reference: |
HP:0012126 |
Genes and Diseases: | | Child Nodes: | Sister Nodes: | ..Gastric leiomyosarcoma (HP:0031025)
| ..Gastric lymphoma (HP:0045038)
| ..Hamartomatous stomach polyps (HP:0004795)
| ..Multiple gastric polyps (HP:0004394)
| Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: | HPO disease - gene - phenotype less frequent non-typical associations: | HP:0012126 | HP:0012126 | Stomach cancer | 0 | AAGAB CL E G H | 79719 | 25662 | ORPHA:79501 | Punctate palmoplantar keratoderma type 1 | HP:0040284 - Very rare | | | 7 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | APC CL E G H | 324 | 583 | OMIM:613659 | Gastric cancer, somatic | . | | | 3179 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | BLM CL E G H | 641 | 1058 | ORPHA:125 | Bloom syndrome | HP:0040284 - Very rare | | | 314 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | BMPR1A CL E G H | 657 | 1076 | ORPHA:440437 | Familial colorectal cancer Type X | HP:0040284 - Very rare | | | 385 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | BUB1 CL E G H | 699 | 1148 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 5 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | BUB1B CL E G H | 701 | 1149 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 76 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | BUB3 CL E G H | 9184 | 1151 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | CASP10 CL E G H | 843 | 1500 | OMIM:613659 | Gastric cancer, somatic | . | | | 87 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | CDH1 CL E G H | 999 | 1748 | OMIM:137215 | Gastric cancer, hereditary diffuse | . | | | 1003 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | CDKN2A CL E G H | 1029 | 1787 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040283 - Occasional | | | 289 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | CEP57 CL E G H | 9702 | 30794 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 17 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | CHEK2 CL E G H | 11200 | 16627 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040283 - Occasional | | | 833 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | CHEK2 CL E G H | 11200 | 16627 | OMIM:609265 | LI-FRAUMENI SYNDROME 2; LFS2 | | | | 833 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | COL14A1 CL E G H | 7373 | 2191 | ORPHA:79501 | Punctate palmoplantar keratoderma type 1 | HP:0040284 - Very rare | | | 2 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | ERBB2 CL E G H | 2064 | 3430 | OMIM:613659 | Gastric cancer, somatic | . | | | 77 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | FGFR2 CL E G H | 2263 | 3689 | OMIM:613659 | Gastric cancer, somatic | . | | | 175 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | IL1B CL E G H | 3553 | 5992 | OMIM:613659 | Gastric cancer, somatic | . | | | 2 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | IL1RN CL E G H | 3557 | 6000 | OMIM:613659 | Gastric cancer, somatic | . | | | 40 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | IRF1 CL E G H | 3659 | 6116 | OMIM:613659 | Gastric cancer, somatic | . | | | 2 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | KLF6 CL E G H | 1316 | 2235 | OMIM:613659 | Gastric cancer, somatic | . | | | 18 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | KRAS CL E G H | 3845 | 6407 | OMIM:613659 | Gastric cancer, somatic | . | | | 196 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | MDM2 CL E G H | 4193 | 6973 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040283 - Occasional | | | 1 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | MSH3 CL E G H | 4437 | 7326 | ORPHA:480536 | MSH3-related attenuated familial adenomatous polyposis | HP:0040282 - Frequent | | | 5 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | MUTYH CL E G H | 4595 | 7527 | OMIM:613659 | Gastric cancer, somatic | . | | | 592 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | PIK3CA CL E G H | 5290 | 8975 | OMIM:613659 | Gastric cancer, somatic | . | | | 162 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | RPS20 CL E G H | 6224 | 10405 | ORPHA:440437 | Familial colorectal cancer Type X | HP:0040284 - Very rare | | | 1 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | SEMA4A CL E G H | 64218 | 10729 | ORPHA:440437 | Familial colorectal cancer Type X | HP:0040284 - Very rare | | | 48 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | STK11 CL E G H | 6794 | 11389 | ORPHA:2869 | Peutz-Jeghers syndrome | HP:0040283 - Occasional | | | 740 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | TP53 CL E G H | 7157 | 11998 | ORPHA:524 | Li-Fraumeni syndrome | HP:0040283 - Occasional | | | 911 | | | HP:0012126 | HP:0012126 | Stomach cancer | 0 | TRIP13 CL E G H | 9319 | 12307 | ORPHA:1052 | Mosaic variegated aneuploidy syndrome | HP:0040283 - Occasional | | | 2 | | |
Genes (29) :AAGAB APC BLM BMPR1A BUB1 BUB1B BUB3 CASP10 CDH1 CDKN2A CEP57 CHEK2 COL14A1 ERBB2 FGFR2 IL1B IL1RN IRF1 KLF6 KRAS MDM2 MSH3 MUTYH PIK3CA RPS20 SEMA4A STK11 TP53 TRIP13
Diseases (10) :ORPHA:79501 OMIM:613659 ORPHA:125 ORPHA:440437 ORPHA:1052 OMIM:137215 ORPHA:524 OMIM:609265 ORPHA:480536 ORPHA:2869 |
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.
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