Gastric ulcer
Symptom Information:
Symptom ID: | HPO:0002592 | ||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) 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) Abnormality of the gastric mucosa(HPO:0004295) Gastric ulcer(HPO:0002592) Peptic ulcer(HPO:0004398) Gastric ulcer(HPO:0002592) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal ulceration and perforation(MedDRA:10018027) Gastric ulcers and perforation(MedDRA:10017847) Gastric ulcer(HPO:0002592) |
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Database Frequency: | 39 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Annular pancreas | (Orphanet:675) |
Arthrogryposis multiplex congenita | (Orphanet:1037) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CREST syndrome | (Orphanet:90290) |
Caroli disease | (Orphanet:53035) |
Coffin-Siris syndrome | (Orphanet:1465) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cystic fibrosis - gastritis - megaloblastic anemia | (Orphanet:2575) |
Deafness - small bowel diverticulosis - neuropathy | (Orphanet:3217) |
Dubin-Johnson syndrome | (Orphanet:234) |
ESOPHAGITIS, EOSINOPHILIC, 1 | (OMIM:610247) |
ESOPHAGITIS, EOSINOPHILIC, 2 | (OMIM:613412) |
Familial advanced sleep-phase syndrome | (Orphanet:164736) |
Gastrocutaneous syndrome | (Orphanet:2069) |
Indolent systemic mastocytosis | (Orphanet:98848) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Intellectual deficit, X-linked, Cantagrel type | (Orphanet:85277) |
Kindler syndrome | (Orphanet:2908) |
Lethal acantholytic epidermolysis bullosa | (Orphanet:158687) |
Mixed connective tissue disease | (Orphanet:809) |
Multiple endocrine neoplasia type 1 | (Orphanet:652) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Neurogenic arthrogryposis multiplex congenita | (Orphanet:1143) |
Oculogastrointestinal muscular dystrophy | (Orphanet:1876) |
Pachydermoperiostosis | (Orphanet:2796) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Reynolds syndrome | (Orphanet:779) |
Rotor syndrome | (Orphanet:3111) |
Systemic mastocytosis | (Orphanet:2467) |
Systemic sclerosis | (Orphanet:90291) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Tremor - nystagmus - duodenal ulcer | (Orphanet:3350) |
Typhoid | (Orphanet:99745) |
Williams syndrome | (Orphanet:904) |
Wolfram syndrome | (Orphanet:3463) |
Wolfram syndrome 2 | (OMIM:604928) |