Neoplasm of the stomach
Symptom Information:
Symptom ID: | HPO:0006753 | ||||||||||||||||||
Synonyms: |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the gastrointestinal tract(HPO:0007378) Neoplasm of the stomach(HPO:0006753) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Abnormality of the stomach(HPO:0002577) Neoplasm of the stomach(HPO:0006753) Neoplasm of the gastrointestinal tract(HPO:0007378) Neoplasm of the stomach(HPO:0006753) MedDRA: Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104) Gastrointestinal neoplasms malignant and unspecified(MedDRA:10017991) Gastrointestinal neoplasms malignancy unspecified NEC(MedDRA:10017994) Neoplasm of the stomach(HPO:0006753) |
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Database Frequency: | 13 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
COLORECTAL CANCER | (OMIM:114500) |
Carney triad | (Orphanet:139411) |
Carney-Stratakis syndrome | (Orphanet:97286) |
Common variable immunodeficiency | (Orphanet:1572) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Familial melanoma | (Orphanet:618) |
Gastrointestinal stromal tumor | (Orphanet:44890) |
Hereditary nonpolyposis colon cancer | (Orphanet:144) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Muir-Torre syndrome | (Orphanet:587) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Pseudomyxoma peritonei | (Orphanet:26790) |
Rothmund-Thomson syndrome | (Orphanet:2909) |