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MIM:613711 - HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3; HSCR3
Xenbase Genes: gdnf
Human Disease Resource: OMIM
MONDO:0013383 - Hirschsprung disease, susceptibility to, 3 |
MONDO:0018309 - Hirschsprung disease |
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MONDO:0013383 - Hirschsprung disease, susceptibility to, 3 |
MONDO:0018309 - Hirschsprung disease |