Genomics England

TTC8

tetratricopeptide repeat domain 8

Panel	Mode of inheritance	Details
Filter panels11 panels
Green in Bardet Biedl syndrome R-numbers: R107 Signed-off version 2.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Bardet-Biedl syndrome 8, 615985
Green in DDG2P Component of the following Super Panels: - Paediatric disorders Signed-off version 3.79	BIALLELIC, autosomal or pseudoautosomal	Phenotypes BARDET-BIEDL SYNDROME TYPE 8 209900, RETINITIS PIGMENTOSA TYPE 51 613464
Green in Fetal anomalies R-numbers: R21, R412 Signed-off version 3.122	BIALLELIC, autosomal or pseudoautosomal	Phenotypes RETINITIS PIGMENTOSA TYPE 51, BARDET-BIEDL SYNDROME TYPE 8
Green in Intellectual disability Component of the following Super Panels: - Childhood onset leukodystrophy - Hypotonic infant - Paediatric disorders R-numbers: R29 Signed-off version 5.343	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Bardet-Biedl syndrome 8, 209900Retinitis pigmentosa 51, 613464, RETINITIS PIGMENTOSA TYPE 51 (RP51)
Green in Limb disorders Component of the following Super Panels: - Paediatric disorders Signed-off version 4.13	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Polydactyly, Bardet-Biedl syndrome 8, 615985
Green in Ophthalmological ciliopathies Component of the following Super Panels: - Paediatric disorders - Rare multisystem ciliopathy Super panel Signed-off version 3.5	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Bardet Biedl syndrome 8
Green in Renal ciliopathies Component of the following Super Panels: - Cystic renal disease - Paediatric disorders - Rare multisystem ciliopathy Super panel Signed-off version 3.3	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Bardet Biedl syndrome 8
Green in Retinal disorders R-numbers: R32 Signed-off version 4.42	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Eye Disorders, Bardet-Biedl syndrome 8, 209900, Retinitis pigmentosa 51, 613464, Retinitis Pigmentosa, Recessive, Retinitis pigmentosa, ?Retinitis pigmentosa 51
Green in Severe early-onset obesity R-numbers: R149 Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Obesity, Bardet-Biedl syndrome 8, OMIM:615985
Green in Skeletal dysplasia Component of the following Super Panels: - Paediatric disorders R-numbers: R104 Signed-off version 4.31	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Polydactyly, Bardet-Biedl syndrome 8, 615985
Green in Unexplained young onset end-stage renal disease R-numbers: R257 Signed-off version 3.11	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Ciliopathy genes associated with cystic kidney disease, Bardet-Biedl syndrome 8 615985