Familial hyperaldosteronism type 3 is an autosomal dominant disorder caused by mutations of the KCNJ5 gene.
Hyperaldosteronism | ||||
Conn syndrome | ||||
Glucocorticoid triggered hypertension | ||||
Hyperaldosteronism type 1 | ||||
Hyperaldosteronism type 2 | ||||
Hyperaldosteronism type 3 | ||||
KCNJ5 | ||||
Hyperaldosteronism type 4 | ||||
1. |
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8. |
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9. |
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None (2013) Primary aldosteronism and potassium channel mutations. |
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13. |
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14. |
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15. |
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16. |
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17. |
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18. |
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19. |
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20. |
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21. |
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22. |
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23. |
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25. |
OMIM.ORG article Omim 613677 |
26. |
Orphanet article Orphanet ID 251274 |