Abnormality of the gastrointestinal tract
Symptom Information:
Symptom ID: | HPO:0011024 | ||||||
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) MedDRA: |
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Database Frequency: | 5 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Bardet-Biedl syndrome 9 | (OMIM:615986) |
Diabetic embryopathy | (Orphanet:1926) |
Fabry disease | (Orphanet:324) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |