An inherited susceptibility or predisposition to developing Hirschsprung disease in which the cause of the disease is a mutation in the EDN3 gene.
Comprehensive, easy-to-understand information about this condition
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Hirschsprung disease, susceptibility to, 1
MONDO:0007723
Hirschsprung disease, susceptibility to, 2
MONDO:0010833
Hirschsprung disease, susceptibility to, 5
MONDO:0010834
Hirschsprung disease, susceptibility to, 6
MONDO:0011741
Hirschsprung disease, susceptibility to, 7
MONDO:0011742
Hirschsprung disease, susceptibility to, 8
MONDO:0012042