CDK13-related disorder

noun

A rare genetic disorder characterised by congenital heart defects, intellectual disability, and characteristic facial features, caused by a mutation in the CDK13 gene.

Similar
CHDFIDD
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Meanings

nounCDK13-related disorder (uncountable)
  1. uncountableA rare genetic disorder characterised by congenital heart defects, intellectual disability, and characteristic facial features, caused by a mutation in the CDK13 gene.

    Synonyms: CHDFIDD

Synonyms & antonyms

nounA rare genetic disorder characterised by congenital heart defects, intellectual disability, and characteristic facial features, caused by a mutation in the CDK13 gene.

Similar
CHDFIDD
Cite this entry
APA

CDK13-related disorder. (n.d.). In WatkinsX Dictionary. Retrieved November 5, 2026, from https://dictionary.watkinsx.com/word/CDK13-related%20disorder

MLA

“CDK13-related disorder.” WatkinsX Dictionary, https://dictionary.watkinsx.com/word/CDK13-related%20disorder. Accessed November 5, 2026.

Chicago

WatkinsX Dictionary, s.v. “CDK13-related disorder,” accessed November 5, 2026, https://dictionary.watkinsx.com/word/CDK13-related%20disorder.

Source: CDK13-related disorder on Wiktionary, CC BY-SA 4.0.