Other hypoparathyroidism

Preferred Label : Other hypoparathyroidism;

Diag associé à un acte (%) : 80.4;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E208;

UMLS CUI

C0348454;

CISMeF manual mappings
- Pseudohypoparathyroidism [ORDO Disease]
Currated CISMeF NLP mapping
- HYPOPARATHYROIDISM [WHO-ART Preferred Term]
- Hypoparathyroidism [MedDRA Preferred Term]
- Pseudohypoparathyroidism [TUV Term]
- Pseudohypoparathyroidism [MedDRA Preferred Term]
- Pseudohypoparathyroidism [TUV Concept]
- hypoparathyroidism [MeSH Descriptor]
- hypoparathyroidism [MeSH concept]
- hypoparathyroidism, nos [SNOMED Notion]
- pseudohypoparathyroidism [MeSH Descriptor]
DO Cross reference
- autosomal dominant hypocalcemia [DO Concept]
Manual NTBT mappings (CISMeF)
- Pseudohypoparathyroidism type 1B [ORDO Disease]
- Pseudohypoparathyroidism type 2 [ORDO Disease]
Orphanet concepts
- Autoimmune hypoparathyroidism [ORDO Disease]
- Autosomal dominant hypocalcemia [ORDO Disease]
- Familial isolated hypoparathyroidism [ORDO Disease]
- Familial isolated hypoparathyroidism due to agenesis of parathyroid gland [ORDO Disease]
- Familial isolated hypoparathyroidism due to impaired PTH secretion [ORDO Disease]
- Rare hypoparathyroidism [ORDO Disease]
- Secondary hypoparathyroidism due to impaired parathormon secretion [ORDO Disease]
See also inter- (CISMeF)
- pseudohypoparathyroidism [Disease (Nov.)]
- pseudopseudohypoparathyroidism [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to NTBT
- hypoparathyroidism [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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