Cytoscape Web
Click node...

Classic Bartter syndrome
1 OMIM reference -
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
Gitelman syndrome
Infantile Bartter syndrome with deafness
Synonym(s):
- Adult Bartter syndrome
- Bartter syndrome type 3
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CLCNKB P51801602023
No signs/symptoms info available.