OBO ID: DOID:0110144
Term Name: Bartter disease type 3 Search Ontology:
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 Bartter disease type 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CLCNKA Bartter syndrome, type 3 607364
CLCNKB Bartter syndrome, type 3 607364
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.