FAM57B

family with sequence similarity 57 member B
OMIM: 615175, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green FAM57B in Retinal disorders

Level 3: Posterior segment abnormalities
Level 2: Ophthalmological disorders
Version 2.285
Latest signed off version: v2.195 (5 Aug 2021)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
  • Literature
Phenotypes
  • Cone-rod dystrophy, MONDO:0015993
  • Maculopathy
Tags
  • new-gene-name