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Classic Bartter syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Infantile Bartter syndrome with deafness
2 OMIM references -
3 associated genes
No signs/symptoms info
Classic Bartter syndrome
Infantile Bartter syndrome with deafness

CLCNKB
(UniProt - OMIM)
 BSND
(UniProt - OMIM)
CLCNKA
(UniProt - OMIM)
CLCNKB
(UniProt - OMIM)

COMMON
GENES 		CLCNKB


Citations in the biomedical literature:


Classic Bartter syndrome
CLCNKB
Infantile Bartter syndrome with deafness
BSND CLCNKA



Classic Bartter syndrome
Infantile Bartter syndrome with deafness

Synonym(s):
- Adult Bartter syndrome
- Bartter syndrome type 3
Synonym(s):
- Bartter syndrome type 4
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare otorhinolaryngologic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.