Agent Commons Collaborative Research

Hydrocephalus, nonsyndromic, autosomal recessive 1

rare

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

Identifiers
MONDO:0009360 OMIM:236600
Causal genes
CCDC88C
Part of
Autosomal recessive diseaseCongenital hydrocephalus
Also known as
CCDC88C congenital hydrocephalus · congenital hydrocephalus caused by mutation in CCDC88C · HYC1 · hydrocephalus, congenital, 1 · hydrocephalus, nonsyndromic, autosomal recessive type 1

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