NTNG2

netrin G2
ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green NTNG2 in Angelman Rett like syndromes Level 2: Dysmorphic and congenital abnormality syndromes Version 1.14	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia, MIM# 618718
Green NTNG2 in Mendeliome Version 1.3801	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Intellectual disability autism dysmorphic features Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia, MIM# 618718
Green NTNG2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.508	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Intellectual disability autism dysmorphic features Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia, MIM# 618718
Amber NTNG2 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.111	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert Review Phenotypes Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia, MIM# 618718
Green NTNG2 in Prepair 1000+ Level 2: Screening Version 2.15	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia, MIM# 618718