Hypokalemic Periodic Paralysis, Type 2 (HOKPP2)

Alias:
Hokpp2
Paralysis, Hypokalemic, Periodic, Type 2
Periodic Paralysis Hypokalemic 2
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypokalemic Periodic Paralysis, Type 2, also known as hokpp2, is related to hyperkalemic periodic paralysis and myotonia. An important gene associated with Hypokalemic Periodic Paralysis, Type 2 is SCN4A (Sodium Voltage-Gated Channel Alpha Subunit 4), and among its related pathways/superpathways are Neuroscience and L1CAM interactions. Affiliated tissues include skeletal muscle, and related phenotypes are hypokalemia and myopathy
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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3
17
25

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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