Functional abnormality of the gastrointestinal tract
Symptom Information:
| Symptom ID: | HPO:0012719 | |
| Synonyms: |
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| Quality: | ||
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HPO:
MedDRA: |
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| Database Frequency: | 17 / 7739 | |
| Resource: | HPO |
All diseases associated with this symptom:
| Cardiofaciocutaneous syndrome | (Orphanet:1340) |
| Curry-Jones syndrome | (Orphanet:1553) |
| Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
| Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
| Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
| Fabry disease | (Orphanet:324) |
| Hirschsprung disease | (Orphanet:388) |
| Hyperkalemic periodic paralysis | (Orphanet:682) |
| Limited cutaneous systemic sclerosis | (Orphanet:220402) |
| Limited systemic sclerosis | (Orphanet:220407) |
| Liposarcoma | (Orphanet:69078) |
| Myxoid/round cell liposarcoma | (Orphanet:99967) |
| Nasu-Hakola disease | (Orphanet:2770) |
| Non-polyposis Turcot syndrome | (Orphanet:99817) |
| Thrombocytopenia - absent radius | (Orphanet:3320) |
| Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay | (Orphanet:73246) |
| Well-differentiated liposarcoma | (Orphanet:99971) |