Disease #00591

Official abbreviation 618237
Name MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15
OMIM ID 618237
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NDUFAF4
Associated tissues -
Disease features -
Remarks -