pseudopseudohypoparathyroidism

Preferred Label : pseudopseudohypoparathyroidism;

MeSH definition : 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.;

MeSH synonym : pseudo-pseudohypoparathyroidism; pseudo pseudohypoparathyroidism; pseudopseudo-hypoparathyroidism; pseudopseudo-hypoparathyroidisms; pseudopseudo hypoparathyroidism; pseudo-pseudohypoparathyroidisms; pseudopseudohypoparathyroidisms; albright hereditary osteodystrophy without multiple hormone resistance;

MeSH annotation : do not confuse with PSEUDOHYPOPARATHYROIDISM of which it is an incomplete form;

Details

Origin ID

D011556;

UMLS CUI

C0033835;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Currated CISMeF NLP mapping
- Albright Hereditary Osteodystrophy without Multiple Hormone Resistance [NCIt concept]
- Hypercalcemia [ICD-9 code]
- Pseudohypoparathyroidism (disorder) [SNOMED CT concept]
- Pseudopseudohypoparathyroidism [ICD-11 More detail]
- Pseudopseudohypoparathyroidism [OMIM Phenotype]
- Pseudopseudohypoparathyroidism [ORDO Disease]
- Pseudopseudohypoparathyroidism (disorder) [SNOMED CT concept]
- normocalcemic pseudohypoparathyroidism [SNOMED Notion]
- pseudopseudohypoparathyroidism [DO Concept]
DO Cross reference
- pseudopseudohypoparathyroidism [DO Concept]
Manual NTBT mappings (CISMeF)
- Developmental anomaly of metabolic origin [ORDO Disease]
- Genetic hypoparathyroidism [ORDO Disease]
- Genetic renal tubular disease [ORDO Disease]
- Rare hypoparathyroidism [ORDO Disease]
- Rare renal tubular disease [ORDO Disease]
Ne pas confondre avec
- Pseudohypoparathyroidism [ORDO Disease]
ORDO relation(s)
- Pseudopseudohypoparathyroidism [ORDO Disease]
Record concept(s)
- pseudopseudohypoparathyroidism [MeSH concept]
See also
- GTP-Binding protein alpha subunits, gs [MeSH Descriptor]
See also inter- (CISMeF)
- HYPOPARATHYROIDISM [WHO-ART Preferred Term]
- Hypocalcemia [ICD-9 code]
- Hypoparathyroidism [ICD-10 category]
- Hypoparathyroidism [ICD-9 code]
- Hypoparathyroidism [ICD-10 category (who)]
- Hypoparathyroidism [HPO term]
- Hypoparathyroidism [MedDRA Preferred Term]
- Hypoparathyroidism [NCIt concept]
- Hypoparathyroidism (disorder) [SNOMED CT concept]
- Other hypoparathyroidism [ICD-10 Sub-category]
- Other hypoparathyroidism [ICD-10 Sub-category (who)]
- Pseudohypoparathyroidism [ORDO Disease]
- Pseudohypoparathyroidism [ICD-10 Sub-category]
- Pseudohypoparathyroidism [PASCAL descriptor]
- Pseudohypoparathyroidism [NCIt concept]
- Pseudohypoparathyroidism [ICD-10 Sub-category (who)]
- Pseudohypoparathyroidism [HPO term]
- Pseudohypoparathyroidism [MedDRA Preferred Term]
- Pseudohypoparathyroidism [TUV Concept]
- Pseudohypoparathyroidism [TUV Term]
- Pseudohypoparathyroidism type 1B [ORDO Disease]
- Pseudohypoparathyroidism type 2 [ORDO Disease]
- Pseudohypoparathyroidism, type ia [OMIM Phenotype]
- hypoparathyroidism [Disease (Nov.)]
- hypoparathyroidism, nos [SNOMED Notion]
- pseudohypoparathyroidism [Disease (Nov.)]
- pseudohypoparathyroidism [DO Concept]
- pseudohypoparathyroidism, nos [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Albright Hereditary Osteodystrophy without Multiple Hormone Resistance [NCIt concept]
- Pseudopseudohypoparathyroidism [OMIM Phenotype]
- Pseudopseudohypoparathyroidism [ORDO Disease]
- Pseudopseudohypoparathyroidism [ICD-11 More detail]
- Pseudopseudohypoparathyroidism (disorder) [SNOMED CT concept]
- normocalcemic pseudohypoparathyroidism [SNOMED Notion]
- pseudopseudohypoparathyroidism [DO Concept]

Keyword's position in hierarchy(ies) :

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