Bartter Disease Type 2 C1855849
A kidney disorder caused by a genetic defect affecting salt and potassium handling. Often presents in early infancy with failure to thrive and dehydration. Management involves electrolyte supplements and careful fluid monitoring.
Key facts at a glance
- ICD-10
- Q63.9
- ICD-11
- LA00.0
- Body system
- renal
- Severity
- severe
- Chronic
- true
Medication Comparisons
Compare medications used to treat Bartter Disease Type 2 C1855849. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy