MeSH Browser

MeSH Heading: Pseudopseudohypoparathyroidism
Tree Number(s): C05.116.198.709.628; C16.320.565.618.815.815; C18.452.104.709.628; C18.452.174.766.815; C18.452.648.618.815.815
Unique ID: D011556
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D011556
Annotation: do not confuse with PSEUDOHYPOPARATHYROIDISM of which it is an incomplete form
Scope Note: A form of PSEUDOHYPOPARATHYROIDISM characterized by the same features except for the abnormal response to hormones such as PARATHYROID HORMONE. It is associated with paternally inherited mutant alleles of the ALPHA CHAIN OF STIMULATORY G PROTEIN.
Entry Term(s): Albright Hereditary Osteodystrophy without Multiple Hormone Resistance; Pseudo-Pseudohypoparathyroidism; Pseudopseudo-Hypoparathyroidism
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: 2015/11/24

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

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complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

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enzymology (EN)

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history (HI)

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metabolism (ME)

microbiology (MI)

mortality (MO)

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prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Pseudopseudohypoparathyroidism MeSH Descriptor Data 2024