Disease #06975 (COQ10D9 (coenzyme Q10 deficiency, primary, type 9), OMIM:619028)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	COQ10D9
Name	coenzyme Q10 deficiency, primary, type 9
OMIM ID	619028
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COQ5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-11-23 21:23:45 +01:00 (CET)
Date last edited	N/A

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