Genomics England

claudin 19

Panel	Mode of inheritance	Details
Filter panels6 panels
Green in DDG2P Component of the following Super Panels: - Paediatric disorders Signed-off version 4.3	BIALLELIC, autosomal or pseudoautosomal	Phenotypes HYPOMAGNESEMIA 5, RENAL, WITH OCULAR INVOLVEMENT 248190
Green in Likely inborn error of metabolism Component of the following Super Panels: - Childhood onset leukodystrophy - Hypotonic infant - Paediatric disorders - Unexplained death in infancy and sudden unexplained death in childhood R-numbers: R98 Signed-off version 5.6	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Hypomagnesemia 5, renal, with ocular involvement 248190
Green in Nephrocalcinosis or nephrolithiasis R-numbers: R256 Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes hypomagensemia with nephrocalcinosis, Hypomagnesemia 5, renal, with ocular involvement
Green in Renal tubulopathies R-numbers: R198 Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Hypomagnesemia 5, renal, with ocular involvement, 248190
Green in Structural eye disease R-numbers: R36 Signed-off version 3.79	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Hypomagnesemia 5, renal, with ocular involvement, 248190
Green in Unexplained young onset end-stage renal disease R-numbers: R257 Signed-off version 4.4	BIALLELIC, autosomal or pseudoautosomal	Phenotypes hypomagensemia with nephrocalcinosis, Hypomagnesemia 5, renal, with ocular involvement