FNBP4

formin binding protein 4
OMIM: 615265, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red FNBP4 in Structural eye disease Version 3.77 Latest signed off version: v3.0 (22 Mar 2023)	review	BIALLELIC, autosomal or pseudoautosomal	Sources NHS GMS Phenotypes Microphthalmia with Limb anomalies (Classified as variant of unknown significance on OMIM), 206920

Panel

Reviews

Mode of inheritance

Details

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

review

BIALLELIC, autosomal or pseudoautosomal

Microphthalmia with Limb anomalies (Classified as variant of unknown significance on OMIM), 206920