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 9.4
Latest signed off version: v9.0 (6 May 2026)

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