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DO Term : Bartter disease type 3 [DOID:0110144] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36.
  • synonyms:
  • 607364,
  • classic Bartter syndrome,
  • BARTS3,
  • GARD:9659,
  • OMIM:607364,
  • Bartter syndrome type 3,
  • ICD10CM:E26.8
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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