1. Genes and Genomic Entities
  2. FBXL7

FBXL7

F-box and leucine rich repeat protein 7
OMIM: 605656, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red FBXL7 in Primary lymphoedema

Level 3: Lymphatic Disorders
Level 2: Cardiovascular disorders
Version 3.11
Latest signed off version: v3.0 (30 Nov 2022)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Hennekam syndrome
  • lymphoedema