Disease #00594

Official abbreviation 618240
Name MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18; MC1DN18
OMIM ID 618240
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NDUFAF3
Associated tissues -
Disease features -
Remarks -