FBXW4

F-box and WD repeat domain containing 4
OMIM: 608071, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red FBXW4 in Mendeliome


Version 1.1902

review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Split-hand/foot malformation 3 syndrome MIM#246560

Red FBXW4 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.285

review Unknown
Sources
  • Illumina TruGenome Clinical Sequencing Services
  • Expert Review Red
  • UKGTN
  • Expert list
  • Emory Genetics Laboratory
Phenotypes
  • Split-hand/foot malformation 3 syndrome 246560

Red FBXW4 in Hand and foot malformations


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.74

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel
  • review Unknown
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Split-hand/foot malformation 3 syndrome 246560