H3F3B:Ensemblv90

H3 histone family member 3B
OMIM: 601058, ClinGen, DECIPHER

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green H3F3B in Mendeliome Version 1.3802	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Bryant-Li-Bhoj neurodevelopmental syndrome 2 MIM#619721
Green H3F3B in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.309 Component of the following Super Panels: Progressive Neurological Conditions	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Bryant-Li-Bhoj neurodevelopmental syndrome 2 MIM#619721
Green H3F3B in Regression Level 2: Neurology and neurodevelopmental disorders Version 0.601	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Bryant-Li-Bhoj neurodevelopmental syndrome 2 MIM#619721
Green H3F3B in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.508	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genetic Health Queensland Victorian Clinical Genetics Services Phenotypes Bryant-Li-Bhoj neurodevelopmental syndrome 2 MIM#619721
Green H3F3B in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature Expert Review Green Phenotypes Bryant-Li-Bhoj neurodevelopmental syndrome 2 MIM#619721
Green H3F3B in Regression Level 2: Neurology and neurodevelopmental disorders Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Victorian Clinical Genetics Services Expert Review Green Phenotypes Bryant-Li-Bhoj neurodevelopmental syndrome 2 MIM#619721
Green H3F3B in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Genetic Health Queensland Expert Review Green Phenotypes Bryant-Li-Bhoj neurodevelopmental syndrome 2 MIM#619721