OR2M7

olfactory receptor family 2 subfamily M member 7
Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red OR2M7 in Retinal disorders

Level 3: Posterior segment abnormalities
Level 2: Ophthalmological disorders
Version 4.89
Latest signed off version: v4.0 (22 Mar 2023)

review Not set
Sources
  • NHS GMS
  • Literature
Phenotypes
  • Other (any phenotype with frequency of fewer than eight individuals)