CAMK2G

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Red CAMK2G in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.389	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Intellectual developmental disorder, autosomal dominant 59, MIM#618522
Amber CAMK2G in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert Review Phenotypes Mental retardation, autosomal dominant 59, MIM# 618522
Amber CAMK2G in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert Review Phenotypes Mental retardation, autosomal dominant 59, MIM# 618522

3 panels