Search Ontology:
Human Disease

Bartter disease type 3

Term ID
DOID:0110144
Synonyms
  • BARTS3
  • Bartter syndrome type 3
  • classic Bartter syndrome
Definition
A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/9326936
References
Ontology
Human Disease   ( DOID:0110144 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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