CDK13

cyclin dependent kinase 13
OMIM: 603309, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green CDK13 in Malformations of cortical development

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 1.151

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Congenital heart defects, dysmorphic facial features, and intellectual development disorder 617360

Green CDK13 in Microcephaly Victorian Clinical Genetics Services


Version 0.2

0 reviews Not set
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green CDK13 in Intellectual disability Victorian Clinical Genetics Services

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 0.2

0 reviews Not set
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services

Green CDK13 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 2.393

4 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Expert Review Green
  • BRIDGE study SPEED NEURO Tier1 Gene
Phenotypes
  • Congenital heart defects, dysmorphic facial features, and intellectual development disorder 617360