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DO Term : Bartter disease type 1 [DOID:0110142] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the sodium-potassium-chloride cotransporter-2 gene (SLC12A1) on chromosome 15q21.
  • synonyms:
  • Bartter syndrome type 1,
  • BARTS1,
  • ICD10CM:E26.8,
  • hyperprostaglandin E syndrome 1,
  • Bartter syndrome type 1 antenatal,
  • 601678,
  • hypokalemic alkalosis with hypercalciuria 1 antenatal,
  • OMIM:601678
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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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