LMAN2L

Panel	Reviews	Mode of inheritance	Details
Amber LMAN2L in Mendeliome Version 1.1902	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Mental retardation, autosomal recessive, 52 OMIM #616887 Intellectual developmental disorder, autosomal dominant 69 , MIM# 617863
Amber LMAN2L in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Mental retardation, autosomal recessive, 52 OMIM #616887 Intellectual developmental disorder, autosomal dominant 69 , MIM# 617863

Panel

Reviews

Mode of inheritance

Details

Version 1.1902

review

BOTH monoallelic and biallelic, autosomal or pseudoautosomal

Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review

BOTH monoallelic and biallelic, autosomal or pseudoautosomal

2 panels