Disease #00017

Official abbreviation MC3DN1
Name Mitochondrial complex III deficiency, nuclear type 1, 124000 (3)
OMIM ID 124000
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes BCS1L, UQCRB
Associated tissues -
Disease features -
Remarks -

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