TMX3

thioredoxin related transmembrane protein 3
OMIM: 616102, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber TMX3 in Structural eye disease


Level 2: Ophthalmology
Version 4.40
Latest signed off version: v4.0 (7 Aug 2024)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • Microphthalmia, coloboma, micrognathia, diaphragmatic hernia
  • None