SLC37A3

solute carrier family 37 member 3
Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber SLC37A3 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	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber NHS GMS Literature Phenotypes retinitis pigmentosa, MONDO:0019200 Tags Q2_24_promote_green Q2_24_NHS_review

Panel

Reviews

Mode of inheritance

Details

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

review

BIALLELIC, autosomal or pseudoautosomal