MAP3K7

mitogen-activated protein kinase kinase kinase 7
OMIM: 602614
PanelMode of inheritanceDetails
4 panels
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 6.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Frontometaphyseal dysplasia 2, 617137, FMD2, autosomal dominant FMD, AD-FMD
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
FRONTOMETAPHYSEAL DYSPLASIA 305620, Cardiospondylocarpofacial syndrome
R-numbers: R21, R412
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Cardiospondylocarpofacial syndrome, OMIM:157800, Cardiospondylocarpofacial syndrome, MONDO:0008005, Frontometaphyseal dysplasia 2, OMIM:617137, Frontometaphyseal dysplasia 2, MONDO:0014935
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Frontometaphyseal dysplasia 2, 617137