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DO Term : Bartter disease type 2 [DOID:0110143] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24.
  • synonyms:
  • hyperprostaglandin E syndrome 2,
  • 241200,
  • Bartter syndrome type 2 antenatal,
  • ICD10CM:E26.8,
  • BARTS2,
  • Bartter syndrome type 2,
  • hypokalemic alkalosis with hypercalciuria 2 antenatal,
  • OMIM:241200
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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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