SAMD7

sterile alpha motif domain containing 7
Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green SAMD7 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Macular dystrophy with or without cone dysfunction, MIM# 620762

Green SAMD7 in Macular Dystrophy/Stargardt Disease


Level 2: Ophthalmological disorders
Version 0.45

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Macular dystrophy with or without cone dysfunction, MIM# 620762