| Descriptor English: | Pseudohypoaldosteronism | ||||||
| Descriptor Spanish: |
Seudohipoaldosteronismo
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| Descriptor Portuguese: | Pseudo-Hipoaldosteronismo | ||||||
| Descriptor French: | Pseudohypoaldostéronisme | ||||||
| Entry term(s): |
Familial Hyperpotassemia and Hypertension Familial Hypertensive Hyperkalemia Familial Hypertensive Hyperkalemias Gordon Hyperkalemia Hypertension Syndrome Gordon Hyperkalemia-Hypertension Syndrome Hyperkalemia, Familial Hypertensive Hyperkalemia-Hypertension Syndrome, Gordon Hyperkalemias, Familial Hypertensive Hyperpotassemia and Hypertension, Familial Hypertensive Hyperkalemia, Familial Hypertensive Hyperkalemias, Familial Pseudohypoaldosteronism Type 1 Pseudohypoaldosteronism Type 1, Autosomal Dominant Pseudohypoaldosteronism Type 1, Autosomal Recessive Pseudohypoaldosteronism Type 1s Pseudohypoaldosteronism Type 2 Pseudohypoaldosteronism Type 2s Pseudohypoaldosteronism Type I Pseudohypoaldosteronism Type II Pseudohypoaldosteronism Type IIs Pseudohypoaldosteronism Type Is Pseudohypoaldosteronism, Type I Pseudohypoaldosteronism, Type I, Autosomal Dominant Pseudohypoaldosteronism, Type I, Autosomal Recessive Pseudohypoaldosteronism, Type II Pseudohypoaldosteronisms Pseudohypoaldosteronisms, Type I Pseudohypoaldosteronisms, Type II Syndrome, Gordon Hyperkalemia-Hypertension Type 1, Pseudohypoaldosteronism Type I Pseudohypoaldosteronism Type I, Pseudohypoaldosteronism Type II Pseudohypoaldosteronism Type II Pseudohypoaldosteronisms Type II, Pseudohypoaldosteronism Type IIs, Pseudohypoaldosteronism Type Is, Pseudohypoaldosteronism |
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| Tree number(s): |
C12.050.351.968.419.815.770 C12.200.777.419.815.770 C12.950.419.815.770 C16.320.831.770 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D011546 | ||||||
| Scope note: | A heterogeneous group of disorders characterized by renal electrolyte transport dysfunctions. Congenital forms are rare autosomal disorders characterized by neonatal hypertension, HYPERKALEMIA, increased RENIN activity and ALDOSTERONE concentration. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Pseudohypoaldosteronism can be the result of a defective renal electrolyte transport protein or acquired after KIDNEY TRANSPLANTATION. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Aldosterone (1971-1987) Hyperaldosteronism (1975-1980) Renal Tubular Transport, Inborn Errors (1971-1987) |
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| Public MeSH Note: | 1991; see RENAL TUBULAR TRANSPORT, INBORN ERRORS 1988-90 |
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| History Note: | 1991(1988); use RENAL TUBULAR TRANSPORT, INBORN ERRORS 1988-90 |
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| Related: |
Epithelial Sodium Channels
MeSH Receptors, Mineralocorticoid MeSH | ||||||
| DeCS ID: | 22975 | ||||||
| Unique ID: | D011546 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1987/03/13 | ||||||
| Revision Date: | 2016/06/23 |
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Pseudohypoaldosteronism
- Preferred
Pseudohypoaldosteronism, Type I
- Narrower
Pseudohypoaldosteronism, Type II
- Narrower
Pseudohypoaldosteronism, Type I, Autosomal Recessive
- Narrower
Hyperpotassemia and Hypertension, Familial
- Narrower
Pseudohypoaldosteronism, Type I, Autosomal Dominant
- Narrower
| Concept UI |
M0017948 |
| Scope note | A heterogeneous group of disorders characterized by renal electrolyte transport dysfunctions. Congenital forms are rare autosomal disorders characterized by neonatal hypertension, HYPERKALEMIA, increased RENIN activity and ALDOSTERONE concentration. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Pseudohypoaldosteronism can be the result of a defective renal electrolyte transport protein or acquired after KIDNEY TRANSPLANTATION. |
| Preferred term | Pseudohypoaldosteronism |
| Entry term(s) |
Pseudohypoaldosteronisms |
| Concept UI |
M0529642 |
| Scope note | Rare autosomal disorder of renal electrolyte transport dysfunctions. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Loss of function mutations in EPITHELIAL SODIUM CHANNELS subunits (autosomal dominant) or MINERALOCORTICOID RECEPTORS (autosomal recessive) cause the disorder. Different mutations in EPITHELIAL SODIUM CHANNELS subunits cause Liddle syndrome. |
| Preferred term | Pseudohypoaldosteronism, Type I |
| Entry term(s) |
Pseudohypoaldosteronism Type 1 Pseudohypoaldosteronism Type 1s Pseudohypoaldosteronism Type I Pseudohypoaldosteronism Type Is Pseudohypoaldosteronisms, Type I Type 1, Pseudohypoaldosteronism Type I Pseudohypoaldosteronism Type I, Pseudohypoaldosteronism Type Is, Pseudohypoaldosteronism |
| Concept UI |
M0461207 |
| Scope note | Autosomal dominant syndrome of renal electrolyte transport dysfunctions. The clinical features include salt-sensitive hypertension, renal HYPERKALEMIA without sodium wasting, normal glomerular filtration rate and metabolic acidosis (hyperchloremic acidemia and HYPERCALCIURIA). Wnk1 and Wnk4 mutations are responsible for the disorder. |
| Preferred term | Pseudohypoaldosteronism, Type II |
| Entry term(s) |
Gordon Hyperkalemia Hypertension Syndrome Gordon Hyperkalemia-Hypertension Syndrome Hyperkalemia-Hypertension Syndrome, Gordon Pseudohypoaldosteronism Type 2 Pseudohypoaldosteronism Type 2s Pseudohypoaldosteronism Type II Pseudohypoaldosteronism Type IIs Pseudohypoaldosteronisms, Type II Syndrome, Gordon Hyperkalemia-Hypertension Type II Pseudohypoaldosteronism Type II Pseudohypoaldosteronisms Type II, Pseudohypoaldosteronism Type IIs, Pseudohypoaldosteronism |
| Concept UI |
M0461206 |
| Preferred term | Pseudohypoaldosteronism, Type I, Autosomal Recessive |
| Entry term(s) |
Pseudohypoaldosteronism Type 1, Autosomal Recessive |
| Concept UI |
M0529701 |
| Preferred term | Hyperpotassemia and Hypertension, Familial |
| Entry term(s) |
Familial Hyperpotassemia and Hypertension Familial Hypertensive Hyperkalemia Familial Hypertensive Hyperkalemias Hyperkalemia, Familial Hypertensive Hyperkalemias, Familial Hypertensive Hypertensive Hyperkalemia, Familial Hypertensive Hyperkalemias, Familial |
| Concept UI |
M0461205 |
| Preferred term | Pseudohypoaldosteronism, Type I, Autosomal Dominant |
| Entry term(s) |
Pseudohypoaldosteronism Type 1, Autosomal Dominant |
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