SAMD7

sterile alpha motif domain containing 7
Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green SAMD7 in Retinal disorders


Level 2: Ophthalmology
Version 8.86
Latest signed off version: v8.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
  • Literature
Phenotypes
  • Macular dystrophy with or without cone dysfunction, OMIM:620762
Tags
  • gene-checked