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DO Term : nuclear type mitochondrial complex I deficiency 28 [DOID:0112095] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA13 gene on chromosome 19p13.11.
  • synonyms:
  • MC1DN28,
  • OMIM:618249,
  • 618249
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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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