WormBase Tree Display for DO_term: DOID:0070239
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DOID:0070239 | Name | primary coenzyme Q10 deficiency 2 | |||
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Status | Valid | ||||
Definition | A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the PDSS1 gene on chromosome 10p12.1. | ||||
Synonym | Exact | COQ10D2 | |||
coenzyme Q10 deficiency, primary, 2 | |||||
deafness-encephaloneuropathy-obesity-valvulopathy syndrome | |||||
hearing loss-encephaloneuropathy-obesity-valvulopathy syndrome | |||||
Parent | Is_a | DOID:0050730 | |||
DB_info | Database | OMIM | disease | 614651 | |
Attribute_of | Gene_by_orthology | WBGene00000761 |