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DO Term : primary autosomal recessive microcephaly 17 [DOID:0070288] 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 CIT gene on chromosome 12q24.
  • synonyms:
  • OMIM:617090,
  • MCPH17,
  • 617090
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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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