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Microcephaly 3, primary, autosomal recessive

rare

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CDK5RAP2 gene.

Identifiers
MONDO:0011488 OMIM:604804
Causal genes
CDK5RAP2
Part of
Autosomal recessive primary microcephaly
Also known as
autosomal recessive primary microcephaly caused by mutation in CDK5RAP2 · CDK5RAP2 autosomal recessive primary microcephaly · MCPH3

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