Disease #00327 (COQ10D1 (coenzyme Q10 deficiency, primary, type 1 (COQ10D-1)), OMIM:607426)

Official abbreviation COQ10D1
Name coenzyme Q10 deficiency, primary, type 1 (COQ10D-1)
OMIM ID 607426
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene COQ2
Associated tissues -
Disease features -
Remarks -