DISEASES

Disease-gene associations mined from literature

Human genes for primary autosomal recessive microcephaly 2 with or without cortical malformations

Primary autosomal recessive microcephaly 2 with or without cortical malformations [DOID:0070293]

A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the WDR62 gene on chromosome 19q13.

Synonyms:  primary autosomal recessive microcephaly 2 with or without cortical malformations,  DOID:0070293,  MCPH2