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DO Term : primary autosomal dominant microcephaly 18 [DOID:0070295] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A primary microcephaly that has_material_basis_in heterozygous mutation in the WDFY3 gene on chromosome 4q21.
  • synonyms:
  • 617520,
  • OMIM:617520,
  • MCPH18
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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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