familial hyperparathyroidism - CISMeF

" /> familial hyperparathyroidism - CISMeF

CISMeF

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Familial hyperparathyroidismSNOMED Notion

Preferred Label : familial hyperparathyroidism;

Details

Origin ID

DB-90130;

UMLS CUI

C0271846;

Automatic exact mappings (from CISMeF team)
- Familial Hypocalciuric Hypercalcemia [NCIt concept]
- Familial benign hypercalcaemia [MedDRA LLT]
- Familial benign hypercalcemia [MedDRA LLT]
- Familial hypocalciuric hypercalcaemia [ICD-11 Subcategory]
Currated CISMeF NLP mapping
- Disorders of calcium metabolism [ICD-10 Sub-category]
- Disorders of calcium metabolism [ICD-10 Sub-category (who)]
- Familial hypocalciuric hypercalcaemia [MedDRA Preferred Term]
- Familial hypocalciuric hypercalcemia [ORDO Disease]
- Familial hypocalciuric hypercalcemia [MedDRA LLT]
- Familial hypocalciuric hypercalcemia (disorder) [SNOMED CT concept]
- Familial primary hyperparathyroidism (disorder) [SNOMED CT concept]
- familial hyperparathyroidism [Disease (Nov.)]
- hypocalciuric hypercalcemia, familial, type 1 [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Disorders of calcium metabolism [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Familial hypocalciuric hypercalcemia type 1 [ORDO Disease]
- Familial hypocalciuric hypercalcemia type 2 [ORDO Disease]
- Familial hypocalciuric hypercalcemia type 3 [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Rare genetic parathyroid disease and phosphocalcic metabolism disorder [ORDO Disease]
- Rare parathyroid disease and phosphocalcic metabolism anomaly [ORDO Disease]
Metaterm(s)
- endocrinology [CISMeF Metaterm]
See also inter- (CISMeF)
- calcium metabolism disorder [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial primary hyperparathyroidism (disorder) [SNOMED CT concept]

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01/05/2025

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