Disease #03692 (COQ10D6 (coenzyme Q10 deficiency, primary, type 6 (COQ10D-6)), OMIM:614650)

Official abbreviation COQ10D6
Name coenzyme Q10 deficiency, primary, type 6 (COQ10D-6)
OMIM ID 614650
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene COQ6
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00180941 - - - F yes Turkey white 11y - yes COQ10 oral, renal transplantation COQ10D6 steroid resistant nephrotic syndrome, end stage renal disease, sensorineural deafness ZXDC COQ6 1 1 Güven Toksoy
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