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DO Term : primary autosomal recessive microcephaly 13 [DOID:0070283] 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 CENPE gene on chromosome 4q24.
  • synonyms:
  • OMIM:616051,
  • 616051,
  • MCPH13
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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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