TRIP12

Panel	Reviews	Mode of inheritance	Details
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Green TRIP12 in Autism Level 2: Neurology and neurodevelopmental disorders Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Mental retardation autosomal dominant 49, Clark-Baraitser Syndrome, MIM#617752
Red TRIP12 in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature Expert Review Red Phenotypes Intellectual developmental disorder, autosomal dominant 49, MIM#617752
Amber TRIP12 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Literature Expert Review Amber Phenotypes Intellectual developmental disorder, autosomal dominant 49 MIM#617752

3 panels