FZD2

frizzled class receptor 2
OMIM: 600667
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 4.195
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Omodysplasia 2, OMIM:164745, Autosomal dominant omodysplasia, MONDO:0008123
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 6.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Omodysplasia 2, OMIM:164745, Robinow syndrome
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 6.16
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Omodysplasia 2, OMIM:164745, Robinow syndrome