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DO Term : primary autosomal recessive microcephaly 2 with or without cortical malformations [DOID:0070293] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the WDR62 gene on chromosome 19q13.
  • synonyms:
  • 604317,
  • MCPH2,
  • OMIM:604317
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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