Cerebellar Atrophy, Developmental Delay, and Seizures (CADEDS)

Alias:
Neurodevelopmental Disorders
Cadeds
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cerebellar Atrophy, Developmental Delay, and Seizures, also known as neurodevelopmental disorders, is related to autism spectrum disorder and liang-wang syndrome. An important gene associated with Cerebellar Atrophy, Developmental Delay, and Seizures is KCNMA1 (Potassium Calcium-Activated Channel Subfamily M Alpha 1). The drugs Metamfetamine and Histamine have been mentioned in the context of this disorder. Affiliated tissues include brain and prefrontal cortex, and related phenotypes are eeg abnormality and global developmental delay
Related ID:
MESH:D004827
ICD11:1516623224

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
16
2

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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