Genomics England

LMX1B

LIM homeobox transcription factor 1 beta

Panel	Mode of inheritance	Details
Filter panels8 panels
Green in Arthrogryposis R-numbers: R83 Signed-off version 5.21	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Nail-patella syndrome, 161200, Nail Patella syndrome, NPS
Green in DDG2P Component of the following Super Panels: - Paediatric disorders Signed-off version 3.79	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes NAIL-PATELLA SYNDROME 161200
Green in Fetal anomalies R-numbers: R21, R412 Signed-off version 3.122	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes NAIL-PATELLA SYNDROME
Green in Limb disorders Component of the following Super Panels: - Paediatric disorders Signed-off version 4.13	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Nail-patella syndrome 161200
Green in Proteinuric renal disease R-numbers: R195 Signed-off version 4.0	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Nail-patella syndrome #161200, FSGS, proteinuria, kidney failure, isolated glomerulopathy
Green in Skeletal dysplasia Component of the following Super Panels: - Paediatric disorders R-numbers: R104 Signed-off version 4.31	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Nail-patella syndrome 161200, Nail-patella syndrome 161200
Green in Structural eye disease R-numbers: R36 Signed-off version 3.0	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Nail-patella syndrome, OMIM:161200
Green in Unexplained young onset end-stage renal disease R-numbers: R257 Signed-off version 3.11	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Nail-patella syndrome 161200