SCD5

stearoyl-CoA desaturase 5
OMIM: 608370, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SCD5 in Monogenic hearing loss


Level 2: Audiology
Version 6.22
Latest signed off version: v6.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Deafness, autosomal dominant 79 OMIM:619086
    • deafness, autosomal dominant 79 MONDO:0033668