FZD2

frizzled class receptor 2
OMIM: 600667, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green FZD2 in Skeletal Dysplasia_Fetal


Level 2: Skeletal disorders
Version 0.230

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Omodysplasia 2, OMIM #164745

Green FZD2 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Autosomal dominant omodysplasia MONDO:0008123

Green FZD2 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.305

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Autosomal dominant omodysplasia type 2 164745
  • Autosomal dominant omodysplasia 164745

Green FZD2 in Hand and foot malformations


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.76

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert list
    • Expert Review Green
    Phenotypes
    • Autosomal dominant omodysplasia 164745
    • Autosomal dominant omodysplasia type 2 164745

    Green FZD2 in Fetal anomalies


    Version 1.314

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Autosomal dominant omodysplasia, MONDO:0008123
    • Omodysplasia 2, OMIM:164745