IPO13

importin 13
OMIM: 610411, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber IPO13 in Structural eye disease


Version 3.77
Latest signed off version: v3.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • NHS GMS