FGF9

fibroblast growth factor 9
OMIM: 600921
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.6
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
MULTIPLE SYNOSTOSES SYNDROME TYPE 3 612961
R-numbers: R100
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Multiple synostoses syndrome 3, OMIM:612961
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 6.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Multiple synostoses syndrome 3, OMIM:612961, multiple synostoses syndrome 3, MONDO:0013064