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Metadata
ID	DOID:0112139
Name	nuclear type mitochondrial complex I deficiency 35
Definition	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB10 gene on chromosome 16p13.3. https://pubmed.ncbi.nlm.nih.gov/28040730/
Xrefs	OMIM:619003
Synonyms	MC1DN35 [EXACT]
Parent Relationships	is_a mitochondrial complex I deficiency is_a autosomal recessive disease