FNBP4

formin binding protein 4
OMIM: 615265, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red FNBP4 in Structural eye disease


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

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
Phenotypes
  • Microphthalmia with Limb anomalies (Classified as variant of unknown significance on OMIM), 206920