Hydrocephalus, nonsyndromic, autosomal recessive 2

Definition

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

Also known as 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, MPDZ congenital hydrocephalus — per MONDO

Also identified as

• OMIM 615219 per MONDO
• UMLS C3554691 per MONDO