LAMA5

laminin subunit alpha 5
OMIM: 601033, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green LAMA5 in Mendeliome Version 1.2302	3 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Bent bone dysplasia syndrome 2, MIM# 620076 nephrotic syndrome Presynaptic congenital myasthenic syndrome multisystem syndrome developmental delay
Green LAMA5 in Proteinuria Level 2: Renal and urinary tract disorders Version 0.229 Component of the following Super Panels: Kidneyome_SuperPanel Renal Glomerular Disease_SuperPanel	5 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Nephrotic syndrome, type 26 620049
Red LAMA5 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.302	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Bent bone dysplasia syndrome 2, MIM# 620076
Red LAMA5 in Congenital Myasthenia Level 2: Neurology and neurodevelopmental disorders Version 1.10 Component of the following Super Panels: Neuromuscular Superpanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Royal Melbourne Hospital Phenotypes Presynaptic congenital myasthenic syndrome
Red LAMA5 in Fetal anomalies Version 1.313	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes bent bone dysplasia nephrotic syndrome Presynaptic congenital myasthenic syndrome multisystem syndrome developmental delay