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 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.38
Latest signed off version: v4.0 (22 Mar 2023)

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