Disease #00604

Official abbreviation 618250
Name MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29; MC1DN29
OMIM ID 618250
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TMEM126B
Associated tissues -
Disease features -
Remarks -