CDK13 is on the Developmental Disorders Genotype-Phenotype Database (DDG2P) because variants in the gene have been previously associated with specific developmental phenotypes. Below is a summary of information about the gene and characteristics of the relevant causal variant. Further information can be found in the DDG2P table.

Category Mode Disease Consequence
Confirmed Monoallelic Syndromic Intellectual Disability with or without Congenital Heart Disease All missense/in frame