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MIM:614651 - COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2
Xenbase Genes: pdss1
Human Disease Resource: MIM
MONDO:0013837 - deafness-encephaloneuropathy-obesity-valvulopathy syndrome |
DOID:0070239 - primary coenzyme Q10 deficiency 2 |
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MONDO:0013837 - deafness-encephaloneuropathy-obesity-valvulopathy syndrome |
DOID:0070239 - primary coenzyme Q10 deficiency 2 |