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... > Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Female Urogenital Diseases > Urologic Diseases > Kidney Diseases > Diabetes Insipidus > Diabetes Insipidus, Nephrogenic
... > Urogenital Diseases > Male Urogenital Diseases > Urologic Diseases > Kidney Diseases > Diabetes Insipidus > Diabetes Insipidus, Nephrogenic
Endocrine System Diseases > Pituitary Diseases > Diabetes Insipidus > Diabetes Insipidus, Nephrogenic
... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Hypothalamic Diseases > Pituitary Diseases > Diabetes Insipidus > Diabetes Insipidus, Nephrogenic

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Diabetes Insipidus, Nephrogenic  

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Tipo

  • mesh:Descriptor

Definición

  • A genetic or acquired polyuric disorder characterized by persistent hypotonic urine and HYPOKALEMIA. This condition is due to renal tubular insensitivity to VASOPRESSIN and failure to reduce urine volume. It may be the result of mutations of genes encoding VASOPRESSIN RECEPTORS or AQUAPORIN-2; KIDNEY DISEASES; adverse drug effects; or complications from PREGNANCY. X-linked congenital nephrogenic diabetes insipidus disorders occurring mostly in males and associated with V2 RECEPTOR mutations. Congenital nephrogenic diabetes insipidus associated with mutations of AQUAPORIN-2.

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Etiquetas alternativas

  • Nephrogenic Diabetes Insipidus

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URI

http://data.loterre.fr/ark:/67375/JVR-M4ZMC6HQ-Q

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RDF/XML TURTLE JSON-LD Creado 16/4/94, última modificación 30/6/21