Morphological abnormality of the gastrointestinal tract
Symptom Information:
Symptom ID: | HPO:0012718 | ||
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HPO:
MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: | HPO |
All diseases associated with this symptom:
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Scleroderma | (Orphanet:801) |