Disease #00592

Official abbreviation 618238
Name MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16
OMIM ID 618238
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NDUFAF5
Associated tissues -
Disease features -
Remarks -

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