1. Genes and Genomic Entities
  2. OLFM2

OLFM2

olfactomedin 2
OMIM: 617492, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber OLFM2 in Structural eye disease


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

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • London North GLH
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • Bilateral microphthalmia, short stature and facial dysmorphism
  • No OMIM