Search Ontology:
Human Disease

Bartter disease type 4b

Term ID
DOID:0110146
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 )
Relationships
Other Pages
Genes Involved
Human Gene Zebrafish Ortholog OMIM Term Disease OMIM Phenotype ID
CLCNKABartter syndrome, type 4b, digenicBartter disease type 4b613090
CLCNKBBartter syndrome, type 4b, digenicBartter disease type 4b613090
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Zebrafish Models
No data available