STARD7

StAR related lipid transfer domain containing 7
OMIM: 616712, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber STARD7 in Early onset or syndromic epilepsy

Level 3: Inherited Epilepsy Syndromes
Level 2: Neurology and neurodevelopmental disorders
Version 5.6
Latest signed off version: v5.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Other
    • Literature
    Phenotypes
    • Epilepsy, familial adult myoclonic, 2, 607876
    • Familial adult myoclonic epilepsy-2
    • FAME-2
    Tags
    • STR