hypoparathyroidism

Preferred Label : hypoparathyroidism;

MeSH definition : A condition caused by a deficiency of PARATHYROID HORMONE (or PTH). It is characterized by HYPOCALCEMIA and hyperphosphatemia. Hypocalcemia leads to TETANY. The acquired form is due to removal or injuries to the PARATHYROID GLANDS. The congenital form is due to mutations of genes, such as TBX1; (see DIGEORGE SYNDROME); CASR encoding CALCIUM-SENSING RECEPTOR; or PTH encoding parathyroid hormone.;

MeSH hyponym : idiopathic hypoparathyroidism; Hypoparathyroidism, Idiopathic;

Wikipedia link : https://en.wikipedia.org/wiki/Hypoparathyroidism;

Details

Origin ID

D007011;

UMLS CUI

C0020626;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [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]
Automatic exact mappings (from CISMeF team)
- Hypoparathyroidism [ACR pathology]
- Hypoparathyroidism [ACR pathology]
- Hypoparathyroidism [ACR pathology]
- Hypoparathyroidism [ACR pathology]
- Hypoparathyroidism, CTCAE [NCIt concept]
- Idiopathic hypoparathyroidism [ICD-10 Sub-category]
- Idiopathic hypoparathyroidism [ICD-11 Sub-sub category]
- Idiopathic hypoparathyroidism [ICD-10 Sub-category (who)]
- Idiopathic hypoparathyroidism (disorder) [SNOMED CT concept]
- Idiopathic parathyroidism (disorder) [SNOMED CT concept]
- endocrine/metabolic/nutritional disease other [ICPC-2 Rubric]
- idiopathic parathyroidism [SNOMED Notion]
- parathyroid disorders [MedlinePlus Topic]
CISMeF manual mappings
- Pseudohypoparathyroidism [ORDO Disease]
Currated CISMeF NLP mapping
- HYPOPARATHYROIDISM [WHO-ART Preferred Term]
- Hypoparathyroidism [PASCAL descriptor]
- Hypoparathyroidism [ICD-10 category]
- Hypoparathyroidism [ICD-10 category (who)]
- Hypoparathyroidism [MedDRA Preferred Term]
- Hypoparathyroidism [ICD-11 Category]
- Hypoparathyroidism [ICD-9 code]
- Hypoparathyroidism [NCIt concept]
- Hypoparathyroidism [HPO term]
- Hypoparathyroidism (disorder) [SNOMED CT concept]
- Hypoparathyroidism, unspecified [ICD-10 Sub-category (who)]
- Hypoparathyroidism, unspecified [ICD-10 Sub-category]
- Hypoparathyroidy [HRDO Sign]
- Other hypoparathyroidism [ICD-10 Sub-category]
- Other hypoparathyroidism [ICD-10 Sub-category (who)]
- Pseudohypoparathyroidism [HPO term]
- Pseudohypoparathyroidism [MedDRA Preferred Term]
- Pseudohypoparathyroidism [TUV Concept]
- Pseudohypoparathyroidism [TUV Term]
- hypoparathyroidism [DO Concept]
- hypoparathyroidism [Disease (Nov.)]
- hypoparathyroidism, nos [SNOMED Notion]
DO Cross reference
- hypoparathyroidism [DO Concept]
HPO term
- Hypoparathyroidism [HPO term]
Manual BTNT mappings - CISMeF
- Pseudohypoparathyroidism type 1B [ORDO Disease]
- Pseudohypoparathyroidism type 2 [ORDO Disease]
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]
MedlinePlus topic(s)
- parathyroid disorders [MedlinePlus Topic]
Ne pas confondre avec
- Pseudohypoparathyroidism [ORDO Disease]
Record concept(s)
- hypoparathyroidism [MeSH concept]
- idiopathic hypoparathyroidism [MeSH concept]
Related MeSH Supplementary Concept(s)
- barakat syndrome [MeSH Supplementary Concept]
- dahlberg borer newcomer syndrome [MeSH Supplementary Concept]
- hypercalciuric hypocalcemia, familial [MeSH Supplementary Concept]
- hypoparathyroidism familial isolated [MeSH Supplementary Concept]
- hypoparathyroidism, X-Linked [MeSH Supplementary Concept]
- hypoparathyroidism, autosomal recessive [MeSH Supplementary Concept]
- hypoparathyroidism-retardation-dysmorphism syndrome [MeSH Supplementary Concept]
- parathyroid glands, agenesis of [MeSH Supplementary Concept]
See also
- parathyroid hormone [MeSH Descriptor]
See also inter- (CISMeF)
- pseudohypoparathyroidism [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- HYPOPARATHYROIDISM [WHO-ART Preferred Term]
- Hypoparathyroidism [ICD-9 code]
- Hypoparathyroidism [ICD-10 category]
- Hypoparathyroidism [MedDRA Preferred Term]
- Hypoparathyroidism [ICD-10 category (who)]
- Hypoparathyroidism [HPO term]
- Hypoparathyroidism [PASCAL descriptor]
- Hypoparathyroidism [ICD-11 Category]
- Hypoparathyroidism [NCIt concept]
- Hypoparathyroidism (disorder) [SNOMED CT concept]
- Hypoparathyroidism, unspecified [ICD-10 Sub-category (who)]
- Hypoparathyroidism, unspecified [ICD-10 Sub-category]
- Rare hypoparathyroidism [ORDO Disease]
- hypoparathyroidism [DO Concept]
- hypoparathyroidism [Disease (Nov.)]
- hypoparathyroidism, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- idiopathic hypoparathyroidism [Disease (Nov.)]

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