Pseudohypoaldosteronism type 2A (Q107250): Difference between revisions
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CID11:ID_646091849 | |||||||||||||||
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dki-india-ID_646091849 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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16 August 2026
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Latest revision as of 14:14, 17 August 2026
This is an autosomal dominant disease in which there is an increase in NCC activity leading to short stature, increased blood pressure, increased serum K+ levels, increased urinary calcium excretion and hyperchloremic metabolic acidosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_646091849 |
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| English | Pseudohypoaldosteronism type 2A |
This is an autosomal dominant disease in which there is an increase in NCC activity leading to short stature, increased blood pressure, increased serum K+ levels, increased urinary calcium excretion and hyperchloremic metabolic acidosis. |
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CID11:ID_646091849
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dki-india-ID_646091849
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Concluído
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16 August 2026
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