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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 - distal phalanx of digit 2
MONDO:0016660 - autosomal recessive primary microcephaly