Hirschsprung disease, susceptibility to, 2

MONDO:0010833

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

Also known as: EDNRB Hirschsprung disease, Hirschsprung disease caused by mutation in EDNRB, Hirschsprung disease, susceptibility to, 2, Hirschsprung disease, susceptibility to, type 2, HSCR2, Hirschsprung disease type 2, susceptibility to Hirschsprung disease 2

0 clinical trials for this condition and its sub-types, 0 tagged with Hirschsprung disease, susceptibility to, 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hirschsprung disease, susceptibility to (0)

Including sub-types (0) Tagged with Hirschsprung disease, susceptibility to, 2 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.