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Metadata
ID	DOID:0112099
Name	nuclear type mitochondrial complex I deficiency 12
Definition	A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFA1 gene on chromosome Xq24. https://pubmed.ncbi.nlm.nih.gov/17262856/
Xrefs	MIM:301020
Synonyms	MC1DN12 [EXACT]
Parent Relationships	is_a X-linked recessive disease is_a nuclear type mitochondrial complex I deficiency
Subclass Logical Relationships	has material basis in some X-linked recessive inheritance