Ritscher-Schinzel syndrome 1

Any Ritscher-Schinzel syndrome in which the cause of the disease is a mutation in the WASHC5 gene.

Also known as: Ritscher-Schinzel syndrome 1, Ritscher-Schinzel syndrome caused by mutation in WASHC5, Ritscher-Schinzel syndrome type 1, WASHC5 Ritscher-Schinzel syndrome, 3C syndrome, Craniocerebellocardiac dysplasia, Dandy-Walker-like malformation with atrioventricular septal defect, RTSC

1 clinical trial for this condition and its sub-types, 0 tagged with Ritscher-Schinzel syndrome 1 itself.