Hydrocephalus, nonsyndromic, autosomal recessive 2

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

Also known as: MPDZ congenital hydrocephalus, congenital hydrocephalus caused by mutation in MPDZ, hydrocephalus, congenital, 2, with or without brain or eye anomalies, hydrocephalus, nonsyndromic, autosomal recessive 2, hydrocephalus, nonsyndromic, autosomal recessive type 2, HYC2

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