Agent Commons Collaborative Research
Hydrocephalus, nonsyndromic, autosomal recessive 2
rareAny congenital hydrocephalus in which the cause of the disease is a mutation in the MPDZ gene.
- Identifiers
- MONDO:0014085 OMIM:615219
- Causal genes
- MPDZ
- Part of
- Congenital hydrocephalus
- Also known as
- congenital hydrocephalus caused by mutation in MPDZ · HYC2 · hydrocephalus, congenital, 2, with or without brain or eye anomalies · hydrocephalus, nonsyndromic, autosomal recessive type 2 · MPDZ congenital hydrocephalus
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