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... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Metal Metabolism, Inborn Errors > Pseudohypoparathyroidism > Pseudopseudohypoparathyroidism
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Metal Metabolism, Inborn Errors > Pseudohypoparathyroidism > Pseudopseudohypoparathyroidism
Nutritional and Metabolic Diseases > Metabolic Diseases > Calcium Metabolism Disorders > Pseudohypoparathyroidism > Pseudopseudohypoparathyroidism
Musculoskeletal Diseases > Bone Diseases > Bone Diseases, Metabolic > Pseudohypoparathyroidism > Pseudopseudohypoparathyroidism
Nutritional and Metabolic Diseases > Metabolic Diseases > Bone Diseases, Metabolic > Pseudohypoparathyroidism > Pseudopseudohypoparathyroidism

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Pseudopseudohypoparathyroidism  

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Tipo

  • mesh:Descriptor

Definición

  • A form of PSEUDOHYPOPARATHYROIDISM characterized by the same features except for the abnormal response to hormones such as PARATHYROID HORMONE. It is associated with paternally inherited mutant alleles of the ALPHA CHAIN OF STIMULATORY G PROTEIN.

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Albright Hereditary Osteodystrophy without Multiple Hormone Resistance
  • Pseudo-Pseudohypoparathyroidism
  • Pseudopseudo-Hypoparathyroidism

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-SSMP0XQD-1

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