Disease #00589

Official abbreviation 618235
Name MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13; MC1DN13
OMIM ID 618235
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NDUFA2
Associated tissues -
Disease features -
Remarks -

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