DIP2B

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
No list DIP2B in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Removed Genetic Health Queensland Phenotypes Mental retardation, FRA12A type, MIM# 136630 Tags 5'UTR
Amber DIP2B_FRA12A_CGG STR in Mendeliome Version 1.3512	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Other Phenotypes Intellectual developmental disorder, autosomal dominant, FRA12A type MIM#136630 Tags 5'UTR
Amber DIP2B_FRA12A_CGG STR in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Other Phenotypes Mental retardation, FRA12A type MIM#136630 Tags 5'UTR
Amber DIP2B_FRA12A_CGG STR in Repeat Disorders Version 0.269	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes intellectual disability, FRA12A type MONDO:0007634 Tags paediatric-onset

4 panels