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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

OMIM:604317

Synonyms

MCPH2 [EXACT]

Parent Relationships

is_a primary autosomal recessive microcephaly

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