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

OMIM:618237

Synonyms

MC1DN15 [EXACT]

Parent Relationships

is_a nuclear type mitochondrial complex I deficiency

is_a autosomal recessive disease

Add an item to the term tracker