SUPT16H

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Green SUPT16H in Mendeliome Version 1.3512	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum, MIM# 619480 Intellectual disability Abnormality of the corpus callosum
Green SUPT16H in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.565	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum, MIM# 619480 Intellectual disability Abnormality of the corpus callosum
Green SUPT16H in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum, MIM# 619480 Intellectual disability Abnormality of the corpus callosum

3 panels