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DO Term : nuclear type mitochondrial complex I deficiency 17 [DOID:0112078] 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 NDUFAF6 gene on chromosome 8q22.1.
  • synonyms:
  • OMIM:618239,
  • MC1DN17,
  • 618239
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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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