Narcolepsy 1 (NRCLP1)

Alias:
Narcolepsy-Cataplexy Syndrome
Cataplexy and Narcolepsy
Narcoleptic Syndrome 1
Narcolepsy-Cataplexy
Narcolepsy, Type 1
Gelineau Disease
Nrclp1
Narcolepsy with Cataplexy and/or Hypocretin Deficiency
Gélineau's Syndrome
Narcolepsy Type 1
Cataplexy
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Narcolepsy 1, also known as narcolepsy-cataplexy syndrome, is related to hypersomnia and idiopathic hypersomnia, and has symptoms including hallucinations, hypnagogic and excessive daytime somnolence. An important gene associated with Narcolepsy 1 is HCRT (Hypocretin Neuropeptide Precursor), and among its related pathways/superpathways are Ebola virus infection in host and CTL Mediated Apoptosis. The drugs Anesthetics and Anesthetics, General have been mentioned in the context of this disorder. Affiliated tissues include eye and skeletal muscle, and related phenotypes are hallucinations and cataplexy
Related ID:
MESH:D009290
ICD11:1851015159

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Child
1-5/10000
12
105
43

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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