Disease #00577

Official abbreviation 500014
Name MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 1; MC1DM1
OMIM ID 500014
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MT-ND3
Associated tissues -
Disease features -
Remarks -

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