STARD9

StAR related lipid transfer domain containing 9
OMIM: 614642, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber STARD9 in Mendeliome


Version 1.3664

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Syndromic disorder (MONDO:0002254), STARD9-related

Amber STARD9 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.286

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    • Literature
    Phenotypes
    • Syndromic disorder (MONDO:0002254), STARD9-related