CDK13

cyclin dependent kinase 13
OMIM: 603309, ClinGen, DECIPHER

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Green CDK13 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.430	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, 617360
Green CDK13 in Craniosynostosis Level 2: Dysmorphic and congenital abnormality syndromes Version 1.68	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Phenotypes Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, MIM# 617360
Green CDK13 in Kabuki syndrome Level 2: Dysmorphic and congenital abnormality syndromes Version 0.15	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Phenotypes Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, MIM#617360
Green CDK13 in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, MIM#617360
Amber CDK13 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.295	1 review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder (MIM#617360)
Green CDK13 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.108 Component of the following Super Panels: Progressive Neurological Conditions	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder MIM#617360
Green CDK13 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 Genetic Health Queensland Phenotypes Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, 617360
Green CDK13 in Fetal anomalies Version 1.313	3 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, 617360
Green CDK13 in Speech apraxia Level 2: Neurology and neurodevelopmental disorders Version 1.27	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, MIM# 617360