Hydrocephalus, nonsyndromic, autosomal recessive 1

Any congenital hydrocephalus in which the cause of the disease is a mutation in the CCDC88C gene.

Also known as: CCDC88C congenital hydrocephalus, congenital hydrocephalus caused by mutation in CCDC88C, hydrocephalus, congenital, 1, hydrocephalus, nonsyndromic, autosomal recessive 1, hydrocephalus, nonsyndromic, autosomal recessive type 1, HYC1, hydrocephaly, ventriculomegaly

4 clinical trials for this condition and its sub-types.