Genomics England

ROR2

receptor tyrosine kinase like orphan receptor 2

Panel	Mode of inheritance	Details
Filter panels6 panels
Green in Clefting Component of the following Super Panels: - Paediatric disorders Signed-off version 4.0	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 3.1	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Phenotypes Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR)
Green in Fetal anomalies R-numbers: R21, R412 Signed-off version 3.0	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Phenotypes Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR)
Green in Intellectual disability - microarray and sequencing Component of the following Super Panels: - Childhood onset leukodystrophy - Hypotonic infant - Paediatric disorders R-numbers: R29 Signed-off version 5.0	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Phenotypes Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR)
Green in Limb disorders Component of the following Super Panels: - Paediatric disorders 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)
Green in Skeletal dysplasia Component of the following Super Panels: - Paediatric disorders R-numbers: R104 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)