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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.

Year introduced: 1965(1963)

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Tree Number(s): C05.116.198.709, C16.320.565.618.815, C18.452.104.709, C18.452.174.766, C18.452.648.618.815

MeSH Unique ID: D011547

Entry Terms:

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

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