LMAN2L

Panel	Reviews	Mode of inheritance	Details
Amber LMAN2L in Mendeliome Version 1.3512	1 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 1.410	2 reviews	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 1.3512

1 review

BOTH monoallelic and biallelic, autosomal or pseudoautosomal

Level 2: Neurology and neurodevelopmental disorders
Version 1.410

2 reviews

BOTH monoallelic and biallelic, autosomal or pseudoautosomal

2 panels