Disease #00606

Official abbreviation 618252
Name MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32; MC1DN32
OMIM ID 618252
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NDUFB8
Associated tissues -
Disease features -
Remarks -

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