Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:616080 - MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE; MCPH12

Xenbase Genes: cdk6

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014484 - microcephaly 12, primary, autosomal recessive
MONDO:0016660 - autosomal recessive primary microcephaly