Disease #00576

Official abbreviation 301021
Name MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 30; MC1DN30
OMIM ID 301021
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NDUFB11
Associated tissues -
Disease features -
Remarks -

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