Related MeSH Hierarchy (5)
Diseases [C] » Musculoskeletal Diseases [C05] » Bone Diseases » Bone Diseases, Metabolic » Pseudohypoparathyroidism
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Metal Metabolism, Inborn Errors » Pseudohypoparathyroidism
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Bone Diseases, Metabolic » Pseudohypoparathyroidism
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Calcium Metabolism Disorders » Pseudohypoparathyroidism
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Metal Metabolism, Inborn Errors » Pseudohypoparathyroidism
Description
A hereditary syndrome clinically similar to HYPOPARATHYROIDISM. It is characterized by HYPOCALCEMIA; HYPERPHOSPHATEMIA; and associated skeletal development impairment and caused by failure of response to PARATHYROID HORMONE rather than deficiencies. A severe form with resistance to multiple hormones is referred to as Type 1a and is associated with maternal mutant allele of the ALPHA CHAIN OF STIMULATORY G PROTEIN. MeSH
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Subtype Terms (1)
Pseudopseudohypoparathyroidism
1 approved drug
Phase 4 Indicated Drugs (1)
Phase 2 Indicated Drugs (1)
Organization Involved with Phase 4 Indications (1)
Organization Involved with Phase 3 Indications (3)
Organization Involved with Phase 2 Indications (1)
Organization Involved with Other Experimental Indications (2)
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UMLS Data
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