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MIM:142623 - HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1; HSCR1
Xenbase Genes: gdnf, ret, phox2b, l1cam, edn3
Human Disease Resource: OMIM
MONDO:0007723 - Hirschsprung disease, susceptibility to, 1 |
MONDO:0018309 - Hirschsprung disease |
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MONDO:0007723 - Hirschsprung disease, susceptibility to, 1 |
MONDO:0018309 - Hirschsprung disease |