Visualize Submit Comment

Metadata
ID	DOID:0112077
Name	nuclear type mitochondrial complex I deficiency 15
Definition	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF4 gene on chromosome 6q16.1. https://pubmed.ncbi.nlm.nih.gov/18179882/
Xrefs	MIM:618237
Synonyms	MC1DN15 [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