Neoplasm of the gastrointestinal tract
Symptom Information:
Symptom ID: | HPO:0007378 | |||||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Neoplasm of the gastrointestinal tract(HPO:0007378) 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 gastrointestinal tract(HPO:0007378) |
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Database Frequency: | 11 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Birt-Hogg-Dube syndrome | (Orphanet:122) |
Bloom syndrome | (Orphanet:125) |
Desmoplastic small round cell tumor | (Orphanet:83469) |
Gastrointestinal stromal tumor | (Orphanet:44890) |
Gorlin syndrome | (Orphanet:377) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Neurofibromatosis type 1 | (Orphanet:636) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Pseudomyxoma peritonei | (Orphanet:26790) |
Werner syndrome | (Orphanet:902) |