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Metadata
ID	DOID:0112086
Name	nuclear type mitochondrial complex I deficiency 26
Definition	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA9 gene on chromosome 12p13.32. https://pubmed.ncbi.nlm.nih.gov/22114105/
Xrefs	OMIM:618247
Synonyms	MC1DN26 [EXACT]
Parent Relationships	is_a nuclear type mitochondrial complex I deficiency is_a autosomal recessive disease