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DO Term : primary autosomal recessive microcephaly 22 [DOID:0051033] 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 NCAPD3 gene on chromosome 11q25.

synonyms:
OMIM:617984,
617984

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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