ROR2

receptor tyrosine kinase like orphan receptor 2
OMIM: 602337
PanelMode of inheritanceDetails
6 panels
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, RRS
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 180700, BRACHYDACTYLY, TYPE B1 113000, ROR2-RELATED DISORDERS AR 268310
R-numbers: R21
Signed-off version 1.92
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
ROR2-RELATED DISORDERS AR, BRACHYDACTYLY, TYPE B1, ROBINOW SYNDROME, AUTOSOMAL DOMINANT
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
BRACHYDACTYLY, TYPE B1
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Brachydactyly, type B1 113000, Robinow syndrome, autosomal recessive 268310
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 2.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Brachydactyly, type B1 113000, Robinow syndrome, autosomal recessive 268310