SIRT6

sirtuin 6
OMIM: 606211, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber SIRT6 in Mendeliome


Version 1.2655

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • syndromic disease, MONDO:0002254, SIRT6-related

Amber SIRT6 in Fetal anomalies


Version 1.370

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • syndromic disease, MONDO:0002254, SIRT6-related