hydrocephalus, nonsyndromic, autosomal recessive Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A cerebral degeneration characterized by an abnormal accumulation of cerebrospinal fluid in the ventricles of the brain, leading to progressive enlargement of the head. (Human Disease Ontology, DOID_10908)
External Link http://www.omim.org/entry/236600
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Genes

1 genes associated with the hydrocephalus, nonsyndromic, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CCDC88C coiled-coil domain containing 88C