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DO Term : mitochondrial complex IV deficiency nuclear type 3 [DOID:0070492] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the COX10 gene on chromosome 17p12.
  • synonyms:
  • UMLS_CUI:C5436682,
  • OMIM:619046,
  • 619046,
  • MC4DN3
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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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