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Metadata
ID	DOID:0112097
Name	nuclear type mitochondrial complex I deficiency 33
Definition	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA6 gene on chromosome 22q13.2. https://pubmed.ncbi.nlm.nih.gov/30245030/
Xrefs	MIM:618253
Synonyms	MC1DN33 [EXACT]
Parent Relationships	is_a nuclear type mitochondrial complex I deficiency is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance