Hirschsprung disease, susceptibility to, 1

MONDO:0007723

Also Known As

Hirschsprung diseaseaganglionic megacolonmegacolon, aganglionicHSCR1Hirschsprung disease caused by mutation in RETHirschsprung disease, susceptibility to, 1Hirschsprung disease, susceptibility to, type 1RET Hirschsprung diseasesusceptibility to Hirschsprung disease 1Hirschsprung disease, protection against

Definition

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

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External Resources

OMIM

OMIM:142623 ↗

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