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DO Term : autosomal dominant pseudohypoaldosteronism type 1 [DOID:0060855] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A pseudohypoaldosteronism characterized by Salt wasting resulting from renal unresponsiveness to mineralocorticoids that has_material_basis_in heterozygous mutation in the NR3C2 gene on chromosome 4q31.
  • synonyms:
  • GARD:9145,
  • OMIM:177735,
  • PHA1A,
  • ORDO:756,
  • MESH:D011546,
  • UMLS_CUI:C1449843,
  • autosomal dominant PHA 1,
  • 177735
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Disease

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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