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Metadata
ID	DOID:0070293
Name	primary autosomal recessive microcephaly 2 with or without cortical malformations
Definition	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the WDR62 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/20890279
Xrefs	MIM:604317
Synonyms	MCPH2 [EXACT]
Parent Relationships	is_a primary autosomal recessive microcephaly