OBO ID: DOID:0110146
Term Name: Bartter disease type 4b Search Ontology:
Synonyms:
  • BARTS4B
  • Bartter syndrome, type 4b, digenic
  • neonatal Bartter syndrome type 4B with sensorineural deafness
Definition: A Bartter disease that has_material_basis_in simultaneous mutation in both the CLCNKA and CLCNKB genes. https://www.ncbi.nlm.nih.gov/pubmed/15044642
References:
Ontology: Human Disease   ( DOID:0110146 )
OTHER Bartter disease type 4b PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CLCNKA Bartter syndrome, type 4b, digenic 613090
CLCNKB Bartter syndrome, type 4b, digenic 613090
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None