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hydrocephalus, nonsyndromic, autosomal recessive 1

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Any congenital hydrocephalus in which the cause of the disease is a mutation in the CCDC88C gene.
Uniprot Description A form of congenital hydrocephalus, a disease characterized by onset in utero of enlarged ventricles due to accumulation of ventricular cerebrospinal fluid. Affected individuals may have neurologic impairment. HYC1 inheritance is autosomal recessive.
Mondo Term and Equivalent IDs
MONDO:0009360:  hydrocephalus, nonsyndromic, autosomal recessive 1
GARD:0006682: 
UMLS:C3887608: