Visualize Submit Comment
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

OMIM:301020

Synonyms

MC1DN12 [EXACT]

Parent Relationships

is_a nuclear type mitochondrial complex I deficiency

is_a X-linked recessive disease

Add an item to the term tracker