FBXL7

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

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red FBXL7 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Hennekam lymphangiectasia-lymphedema syndrome

Red FBXL7 in Lymphoedema_syndromic

Level 3: Lymphatic Disorders
Level 2: Cardiovascular disorders
Version 0.12

Component of the following Super Panels:

  • Vascular Malformations SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Hennekam syndrome
    • lymphedema