primary autosomal recessive microcephaly 2 with or without cortical malformations

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Summary

Literature (0)

DOID:0070293 - primary autosomal recessive microcephaly 2 with or without cortical malformations

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

Synonyms: MCPH2,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): primary autosomal recessive microcephaly (is_a)