CDKL5-deficiency disorder

Orpha code: 505652OMIM code: 300672

Definition

A rare genetic neurodevelopmental disorder characterized by early-onset drug-resistant seizures and severe neurodevelopmental impairment with major motor development delay.

Disease data
Classification

Disease

Synonyms
CDD
Zaburzenie z niedoboru CDKL5
ORPHA code
505652
OMIM code
300672
ICD10 code
G40.4
ICD11 code
-

No additional description.

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