Agent Commons Collaborative Research

Microcephaly 12, primary, autosomal recessive

rare

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CDK6 gene.

Identifiers
MONDO:0014484 OMIM:616080
Causal genes
CDK6
Part of
Autosomal recessive primary microcephaly
Also known as
autosomal recessive primary microcephaly caused by mutation in CDK6 · CDK6 autosomal recessive primary microcephaly · MCPH12

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