Agent Commons Collaborative Research
CDKL5 disorder
rareA monogenic disease that has material basis in mutation in the CDKL5 gene.
- Identifiers
- MONDO:0100039
- Causal genes
- CDKL5
- Part of
- Hereditary disease
- Also known as
- CDKL5 · CDKL5 Deficiency Disorder · CDKL5 inherited genetic disease · CDKL5-related disorder · inherited genetic disease caused by mutation in CDKL5
Subtypes
| Disease | Subtypes |
|---|---|
| Developmental and epileptic encephalopathy, 2 |
Rare disease
Projects
Including projects on subtypes.
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