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DO Term : nuclear type mitochondrial complex I deficiency 19 [DOID:0112085] 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 FOXRED1 gene on chromosome 11q24.2.
  • synonyms:
  • OMIM:618241,
  • 618241,
  • MC1DN19
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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