Liddle syndrome
Information
- Disease name
- Liddle syndrome
- Disease ID
- DOID:0050477
- Description
- "A renal tubular transport disease that is characterized by hypertension and hypokalemia caused by dysregulation of epithelial sodium channels causing over expression of the channel." [url:https\://en.wikipedia.org/wiki/Liddle%27s_syndrome]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT03655223 | Enrolling by invitation | Early Check: Expanded Screening in Newborns | October 15, 2018 | December 31, 2025 | |
| NCT06065852 | Recruiting | National Registry of Rare Kidney Diseases | November 6, 2009 | December 31, 2039 |
- Disase is a (Disease Ontology)
- DOID:447
- Cross Reference ID (Disease Ontology)
- GARD:7381
- Cross Reference ID (Disease Ontology)
- MESH:D056929
- Cross Reference ID (Disease Ontology)
- MIM:177200
- Cross Reference ID (Disease Ontology)
- NCI:C84827
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:707749005
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0221043
- Exact Synonym (Disease Ontology)
- Liddle's syndrome
- Exact Synonym (Disease Ontology)
- Pseudoaldosteronism
- OrphaNumber from OrphaNet (Orphanet)
- 526
- MeSH unique ID (MeSH (Medical Subject Headings))
- D056929