Skip to main content

Medical Subject Headings

Search from vocabulary

Content language

Concept information

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

Preferred term

Pseudohypoparathyroidism  

Type

  • Topical Descriptor

Broader concept

Narrower concepts

Related concepts

Entry terms

  • Pseudohypoparathyroidisms, Type Ia
  • Pseudohypoparathyroidisms, Type Ib
  • Pseudohypoparathyroidism, Type Ia
  • Pseudohypoparathyroidism, Type Ib
  • Type Ia Pseudohypoparathyroidism
  • Type Ia Pseudohypoparathyroidisms
  • Type Ib Pseudohypoparathyroidism
  • Type Ib Pseudohypoparathyroidisms

Note

  • do not confuse with PSEUDOPSEUDOHYPOPARATHYROIDISM

Scope note

  • 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.

History note

  • 65(63)

In other languages

URI

http://www.yso.fi/onto/mesh/D011547

Download this concept:

RDF/XML TURTLE JSON-LD Created 1/1/99, last modified 4/5/23