Genomics England

LAMB1

laminin subunit beta 1

Panel	Mode of inheritance	Details
Filter panels8 panels
Green in Adult onset leukodystrophy R-numbers: R62 Signed-off version 5.0	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Phenotypes Lissencephaly 5, OMIM:615191, cobblestone lissencephaly without muscular or ocular involvement, MONDO:0014077
Green in Adult onset neurodegenerative disorder R-numbers: R58 Signed-off version 7.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Lissencephaly 5, OMIM:615191, cobblestone lissencephaly without muscular or ocular involvement, MONDO:0014077
Green in DDG2P Component of the following Super Panels: - Paediatric disorders Signed-off version 5.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes COBBLESTONE BRAIN MALFORMATION WITHOUT MUSCULAR OR OCULAR ABNORMALITIES 615191
Green in Fetal anomalies R-numbers: R21, R412 Signed-off version 5.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Lissencephaly 5, OMIM:615191, Cobblestone lissencephaly without muscular or ocular involvement, MONDO:0014077
Green in Hydrocephalus R-numbers: R86 Signed-off version 5.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Lissencephaly 5, OMIM:615191
Green in Intellectual disability Component of the following Super Panels: - Childhood onset leukodystrophy - Hypotonic infant - Paediatric disorders R-numbers: R29 Signed-off version 8.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Lissencephaly 5, OMIM:615191
Green in Malformations of cortical development Component of the following Super Panels: - Cerebral malformation Signed-off version 7.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Lissencephaly 5 615191
Green in White matter disorders and cerebral calcification - narrow panel Component of the following Super Panels: - Childhood onset leukodystrophy Signed-off version 6.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Lissencephaly 5, OMIM:615191, Cystic leukoencephalopathy