ROR2

receptor tyrosine kinase like orphan receptor 2
OMIM: 602337
PanelMode of inheritanceDetails
5 panels
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Robinow syndrome, autosomal recessive, OMIM:268310
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR)
R-numbers: R21, R412
Signed-off version 4.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR)
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.4
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR)
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 5.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR)