| Descriptor English: | Liddle Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de Liddle
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| Descriptor Portuguese: | Síndrome de Liddle | ||||||
| Descriptor French: | Syndrome de Liddle | ||||||
| Entry term(s): |
Pseudoaldosteronism Syndrome, Liddle |
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| Tree number(s): |
C12.050.351.968.419.815.683 C12.200.777.419.815.683 C12.950.419.815.683 C16.320.831.698 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D056929 | ||||||
| Scope note: | Familial pseudoaldosteronism characterized by autosomal dominant inheritance of hypertension with HYPOKALEMIA; ALKALOSIS; RENIN and ALDOSTERONE level decreases. It is caused by mutations in EPITHELIAL SODIUM CHANNELS beta and gamma subunits. Different mutations in the same EPITHELIAL SODIUM CHANNELS subunits can cause PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification 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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| Public MeSH Note: | 2010 |
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| History Note: | 2010 |
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| Related: |
Epithelial Sodium Channels
MeSH | ||||||
| DeCS ID: | 53532 | ||||||
| Unique ID: | D056929 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2010/01/01 | ||||||
| Date of Entry: | 2009/07/06 | ||||||
| Revision Date: | 2012/07/03 |
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Liddle Syndrome
- Preferred
| Concept UI |
M0533461 |
| Scope note | Familial pseudoaldosteronism characterized by autosomal dominant inheritance of hypertension with HYPOKALEMIA; ALKALOSIS; RENIN and ALDOSTERONE level decreases. It is caused by mutations in EPITHELIAL SODIUM CHANNELS beta and gamma subunits. Different mutations in the same EPITHELIAL SODIUM CHANNELS subunits can cause PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT. |
| Preferred term | Liddle Syndrome |
| Entry term(s) |
Pseudoaldosteronism Syndrome, Liddle |
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