eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hirschsprung disease |
| Comorbidity | C0002726|amyloidosis |
| Sentences | 1 |
| PubMedID- 21687607 | There are three variants of the syndrome: (1) men2a with hirschsprung disease, (2) men2a associated with cutaneous lichen amyloidosis, and (3) familial mtc, in which mtc is the only manifestation. |
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