Disease #00508

Official abbreviation 616111
Name ?Mitochondrial complex III deficiency, nuclear type 9, 616111 (3)
OMIM ID 616111
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene UQCC3
Associated tissues -
Disease features -
Remarks -

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