FN1

PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Spondylometaphyseal Dysplasia with Corner Fractures 184255
Component of the following Super Panels:
  • - Unexplained young onset end-stage renal disease
R-numbers: R195
Signed-off version 4.15
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Glomerulopathy with fibronectin deposits 2, OMIM:601894
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spondylometaphyseal dysplasia, corner fracture type 184255