Term Name:	primary autosomal recessive microcephaly 2 with or without cortical malformations
Synonyms:	MCPH2
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the WDR62 gene on chromosome 19q13.
Ontology:	Human Disease [DOID:0070293]   ( DOID:0070293 )