Disease #00327 (COQ10D-1 (coenzyme Q10 deficiency, primary, type 1 (COQ10D-1)), OMIM:607426)

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	Curator: Johan T. den Dunnen

Official abbreviation	COQ10D-1
Name	coenzyme Q10 deficiency, primary, type 1 (COQ10D-1)
OMIM ID	607426
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COQ2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-02-16 17:29:49 +01:00 (CET)
Date last edited	N/A