FBXL7

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

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red FBXL7 in Mendeliome


Version 2.0

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

Red FBXL7 in Lymphoedema

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

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