Alternating Hemiplegia of Childhood (AHC)

Alias:
Ahc
Alternating Hemiplegia
Hemiplegia, Alternating, of Childhood
Alternating Hemiplegia Syndrome
Hemiplegia, Crossed
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Alternating Hemiplegia of Childhood, also known as ahc, is related to familial hemiplegic migraine and episodic ataxia, type 6, and has symptoms including hemiplegia, hemiplegia, flaccid and hemiplegia, transient. An important gene associated with Alternating Hemiplegia of Childhood is ATP1A2 (ATPase Na+/K+ Transporting Subunit Alpha 2), and among its related pathways/superpathways are Infectious disease and Transport of inorganic cations/anions and amino acids/oligopeptides. The drugs Glycerin and Sodium oxybate have been mentioned in the context of this disorder. Affiliated tissues include spinal cord and eye, and related phenotypes are abnormality of the gastrointestinal tract and gastrointestinal dysmotility
Related ID:
MESH:C536589

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
1-9/1000000
39
360
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Medical Symptom

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

Gene & Mutation

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No data available

Related Drugs

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CAS Number
Status
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No data available

Disease Model

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

References Literature

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PMID
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IF
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