FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Bartter disease type 4b ID (Ontology) DOID:0110146 (Human Disease)
Definition A Bartter disease that has_material_basis_in simultaneous mutation in both the CLCNKA and CLCNKB genes.
Also Known As "BARTS4B" ; "Bartter syndrome, type 4b, digenic" ; "neonatal Bartter syndrome type 4B with sensorineural deafness"
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 Genes
 Bartter disease type 4b       1
 for disease ribbon | Bartter disease type 4b       1
 model of | Bartter disease type 4b       1
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monogenic disease________________
renal tubular transport disease__|
                                 Bartter disease
                                  |__Bartter disease type 4b  1 rec.
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Synonyms
  • "BARTS4B" EXACT OMO:0003012
    "Bartter syndrome, type 4b, digenic" EXACT
    "neonatal Bartter syndrome type 4B with sensorineural deafness" EXACT
Secondary IDs
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ICD10CM:E26.8
MIM:613090