FBXL7:Ensemblv90

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

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red FBXL7 in Mendeliome


Version 1.3802

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Hennekam lymphangiectasia-lymphedema syndrome MONDO:0016256

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

    Red FBXL7 in Lymphoedema_syndromic

    Level 3: Lymphatic Disorders
    Level 2: Cardiovascular disorders
    Version 1.0

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