SCD5

stearoyl-CoA desaturase 5
OMIM: 608370, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SCD5 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Deafness, autosomal dominant 79, MIM#619086

Red SCD5 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.194

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Deafness, autosomal dominant 79, MIM#619086