Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for DO_term: DOID:0070239

expand all nodes | collapse all nodes | view schema

Name Class

DOID:0070239Nameprimary coenzyme Q10 deficiency 2
StatusValid
DefinitionA primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the PDSS1 gene on chromosome 10p12.1.
SynonymExactCOQ10D2
coenzyme Q10 deficiency, primary, 2
deafness-encephaloneuropathy-obesity-valvulopathy syndrome
hearing loss-encephaloneuropathy-obesity-valvulopathy syndrome
ParentIs_aDOID:0050730
DB_infoDatabaseOMIMdisease614651
Attribute_ofGene_by_orthologyWBGene00000761