Bartter Syndrome Type 4

Alias:
Bartter Syndrome with Sensorineural Deafness
Bartter Syndrome with Sensorineural Hearing Loss
Bartter Syndrome Type Iv
Bartter Syndrome, Type 4a
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Bartter Syndrome Type 4, also known as bartter syndrome with sensorineural deafness, is related to bartter syndrome, type 4b, neonatal, with sensorineural deafness and hypokalemia, and has symptoms including polyuria An important gene associated with Bartter Syndrome Type 4 is BSND (Barttin CLCNK Type Accessory Subunit Beta), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Ion channel transport. Affiliated tissues include kidney, and related phenotypes are hypokalemia and hyperaldosteronism
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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3
20
14

Medical Symptom

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Description
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Gene & Mutation

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Related Drugs

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Disease Model

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MGI
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Publications
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References Literature

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