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Summary Literature (0)
MIM:615219 - HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2

Xenbase Genes: mpdz

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014085 - hydrocephalus, nonsyndromic, autosomal recessive 2
MONDO:0016349 - congenital hydrocephalus

Disease Ontology (DO):
DOID:10908 - hydrocephalus