SIPA1L3

signal induced proliferation associated 1 like 3
OMIM: 616655, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber SIPA1L3 in Bilateral congenital or childhood onset cataracts

Level 3: Anterior segment abnormalities
Level 2: Ophthalmological disorders
Version 4.12
Latest signed off version: v4.0 (22 Mar 2023)

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • ?Cataract 45
Tags
  • watchlist