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coenzyme Q10 deficiency

Disease Summary
Associated Targets (9)
Tbio

8

Tchem

1


GARD Rare
Mondo Description A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency.
Disease Ontology Description A mitochondrial metabolism disease that is characterized by a deficiency of CoQ10 resulting from reduced biosynthesis.
Mondo Term and Equivalent IDs
MONDO:0018151:  coenzyme Q10 deficiency
GARD:0010423: 
MESH:C564403: 
NCIT:C142083: 
OMIMPS:607426: 
Orphanet:35656: 
SCTID:724575009: 
UMLS:C1843920: 
UMLS:CN229570: