Diseases

Pseudohypoparathyroidism

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.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

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.

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Synonyms

19 entry terms
  • Pseudohypoparathyroidisms
  • Albright Hereditary Osteodystrophy
  • Albright Hereditary Osteodystrophy with Multiple Hormone Resistance
  • PHD Ib
  • PHD1b
  • PHP Ia
  • PHPIa
  • Pseudohypoparathyroidism Type 1B
  • Pseudohypoparathyroidism, Type Ia
  • Pseudohypoparathyroidism, Type Ib
  • Hereditary Osteodystrophy, Albright
  • Osteodystrophy, Albright Hereditary
  • Pseudohypoparathyroidism Type 1Bs
  • Pseudohypoparathyroidisms, Type Ia
  • Pseudohypoparathyroidisms, Type Ib
  • Type Ia Pseudohypoparathyroidism
  • Type Ia Pseudohypoparathyroidisms
  • Type Ib Pseudohypoparathyroidism
  • Type Ib Pseudohypoparathyroidisms

MeSH Record

Aspects Covered

34 allowable subheadings

Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.

MeSH Record

Indexing Annotation

do not confuse with PSEUDOPSEUDOHYPOPARATHYROIDISM

MeSH Record

History Note

65(63)

MeSH Hierarchy

Tree Numbers

  1. C05w.116w.198w.709w
  2. C16w.320w.565w.618w.815w
  3. C18.452w.104w.709w
  4. C18.452w.174w.766w
  5. C18.452w.648w.618w.815w

AMA Style

References

  1. National Library of Medicine. Pseudohypoparathyroidism. Medical Subject Headings (MeSH). 2026. Unique ID D011547. http://id.nlm.nih.gov/mesh/2026/D011547
  2. Pseudohypoparathyroidism. In: Wikipedia. https://en.wikipedia.org/wiki/Pseudohypoparathyroidism
  3. Pseudohypoparathyroidism. In: Wikidata. https://www.wikidata.org/wiki/Q819207