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

BSND CLCNKB
CLCNKA
CLCNKB


COMMON
GENES
CLCNKB



Citations in the biomedical literature:


Infantile Bartter syndrome with deafness
BSND CLCNKA CLCNKB
Classic Bartter syndrome



Infantile Bartter syndrome with deafness
Classic Bartter syndrome

Synonym(s):
- Bartter syndrome type 4

Synonym(s):
- Adult Bartter syndrome
- Bartter syndrome type 3

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare otorhinolaryngologic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic 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:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.