"Pseudohypoparathyroidism" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
Descriptor ID |
D011547
|
MeSH Number(s) |
C05.116.198.709 C16.320.565.618.815 C18.452.104.709 C18.452.174.766 C18.452.648.618.815
|
Concept/Terms |
Pseudohypoparathyroidism, Type Ib- Pseudohypoparathyroidism, Type Ib
- Pseudohypoparathyroidisms, Type Ib
- Type Ib Pseudohypoparathyroidism
- Type Ib Pseudohypoparathyroidisms
- PHD1b
- PHD Ib
- PHD Ibs
Pseudohypoparathyroidism, Type Ia- Pseudohypoparathyroidism, Type Ia
- Pseudohypoparathyroidisms, Type Ia
- Type Ia Pseudohypoparathyroidism
- Type Ia Pseudohypoparathyroidisms
- Albright Hereditary Osteodystrophy with Multiple Hormone Resistance
- PHP Ia
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Below are MeSH descriptors whose meaning is more general than "Pseudohypoparathyroidism".
Below are MeSH descriptors whose meaning is more specific than "Pseudohypoparathyroidism".
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