SIRT6

sirtuin 6
OMIM: 606211, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber SIRT6 in Mendeliome


Version 1.4184

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

Amber SIRT6 in Fetal anomalies


Version 1.520

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