MeSH Browser

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 1B; 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: 2023/04/05

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0566696
Terms: Pseudohypoparathyroidism, Type Ib Preferred Term
Term UI T808402
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); PHD Ib
Term UI T817671
Date02/09/2012
LexicalTag NON
ThesaurusID NLM (2013); PHD1b
Term UI T817672
Date02/09/2012
LexicalTag ABB
ThesaurusID NLM (2013); Pseudohypoparathyroidism Type 1B
Term UI T767951
Date03/25/2010
LexicalTag NON
ThesaurusID

Concept UI: M0570744
Scope Note: A syndrome characterized by variable features such as short stature, obesity, round face, subcutaneous ossifications, and BRACHYDACTYLY. It is associated with resistance to PARATHYROID HORMONE and THYROTROPIN. The autosomal dominant inherited form (PSEUDOHYPOPARATHYROIDISM, TYPE IA) is caused by mutations in the GNAS gene. OMIM: 103580.
Terms: Pseudohypoparathyroidism, Type Ia Preferred Term
Term UI T817650
Date02/09/2012
LexicalTag NON
ThesaurusID OMIM (2013); PHPIa
Term UI T001009889
Date03/09/2020
LexicalTag NON
ThesaurusID NLM (2021); Albright Hereditary Osteodystrophy
Term UI T001009888
Date03/09/2020
LexicalTag EPO
ThesaurusID NLM (2021); PHP Ia
Term UI T817651
Date02/09/2012
LexicalTag ABB
ThesaurusID OMIM (2013); Albright Hereditary Osteodystrophy with Multiple Hormone Resistance
Term UI T817653
Date02/09/2012
LexicalTag EPO
ThesaurusID ORD (2010)

Pseudohypoparathyroidism MeSH Descriptor Data 2025