Hydrocephalus, nonsyndromic, autosomal recessive 1

Definition

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 — per MONDO

Also identified as

• OMIM 236600 per MONDO
• UMLS C3887608 per MONDO