Concept information
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Genetic Diseases, Inborn
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Pseudohypoparathyroidism
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Metabolic Diseases
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Pseudohypoparathyroidism
Preferred term
Pseudopseudohypoparathyroidism
Type
-
mesh:Descriptor
Definition
- 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.
Broader concept
Entry terms
- Albright Hereditary Osteodystrophy without Multiple Hormone Resistance
- Pseudo-Pseudohypoparathyroidism
- Pseudopseudo-Hypoparathyroidism
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Pseudo-pseudo-hypoparathyroidie
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Pseudo-pseudohypoparathyroidie
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Pseudopseudohypoparathyroïdie
URI
http://data.loterre.fr/ark:/67375/JVR-SSMP0XQD-1
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