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Pseudohypoparathyroidism MeSH Descriptor Data 2021


MeSH Heading
Pseudohypoparathyroidism
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
Unique ID
D011547
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D011547
Annotation
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.
Entry Term(s)
Albright Hereditary Osteodystrophy
Albright Hereditary Osteodystrophy with Multiple Hormone Resistance
PHD Ib
PHD1b
PHP Ia
PHPIa
Pseudohypoparathyroidism, Type Ia
Pseudohypoparathyroidism, Type Ib
See Also
GTP-Binding Protein alpha Subunits, Gs
Public MeSH Note
65
History Note
65(63)
Date Established
1965/01/01
Date of Entry
1999/01/01
Revision Date
2020/05/27
Pseudohypoparathyroidism Preferred
Pseudohypoparathyroidism, Type Ib Narrower
Pseudohypoparathyroidism, Type Ia Narrower
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