PLXNA2

Panel	Reviews	Mode of inheritance	Details
Amber PLXNA2 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Intellectual disability Abnormality of the face Failure to thrive Abnormal heart morphology
Amber PLXNA2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Other Literature Phenotypes Intellectual disability Abnormality of the face Failure to thrive Abnormal heart morphology

Panel

Reviews

Mode of inheritance

Details

Version 1.1902

review

BIALLELIC, autosomal or pseudoautosomal

Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review

BIALLELIC, autosomal or pseudoautosomal

2 panels