KMT5B

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green KMT5B in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.205	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Victorian Clinical Genetics Services Phenotypes Mental retardation, autosomal dominant 51, MIM#617788
Green KMT5B in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Mental retardation, autosomal dominant 51
Amber KMT5B in Overgrowth Level 2: Dysmorphic and congenital abnormality syndromes Version 1.14	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Mental retardation, autosomal dominant 51, MIM#617788
Green KMT5B 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 Green Expert list Phenotypes Mental retardation, autosomal dominant 51, MIM#617788
Red KMT5B in Fetal anomalies Version 1.313	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Genomics England PanelApp Expert list Phenotypes Mental retardation, autosomal dominant 51, MIM#617788

5 panels