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DO Term : primary autosomal recessive microcephaly 5 [DOID:0070280] 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 ASPM gene on chromosome 1q31.
  • synonyms:
  • MCPH5,
  • 608716,
  • OMIM:608716
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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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