Term Name:	primary autosomal recessive microcephaly 12
Synonyms:	MCPH12
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CDK6 gene on chromosome 7q21.
Ontology:	Human Disease [DOID:0070284]   ( DOID:0070284 )