Hirschsprung disease, susceptibility to, 1

MONDO:0007723

An inherited susceptibility or predisposition to developing Hirschsprung disease in which the cause of the disease is a mutation in the RET gene.

Also known as: Hirschsprung disease, aganglionic megacolon, megacolon, aganglionic, HSCR1, Hirschsprung disease caused by mutation in RET, Hirschsprung disease, susceptibility to, 1, Hirschsprung disease, susceptibility to, type 1, RET Hirschsprung disease

0 clinical trials for this condition and its sub-types, 0 tagged with Hirschsprung disease, susceptibility to, 1 itself.

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