hypocalciuric hypercalcemia, familial, type 1

Preferred Label : hypocalciuric hypercalcemia, familial, type 1;

MeSH synonym : hypercalcemia, familial benign type 1; familial benign hypercalcemia type 1; familial hypocalciuric hypercalcemia; hypercalcemia, familial benign; familial benign hypercalcemia 1; hypocalciuric hypercalcemia, familial, type I;

Détails

Origin ID

C537145;

UMLS CUI

C0342637;

Automatic exact mappings (from CISMeF team)
- Familial Hypocalciuric Hypercalcemia [NCIt concept]
- Familial benign hypercalcemia [MedDRA LLT]
- Familial hypocalciuric hypercalcaemia [ICD-11 Subcategory]
- Hypocalciuric hypercalcemia, familial, type I [OMIM Phenotype]
- familial hypocalciuric hypercalcemia 1 [DO Concept]
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 hypocalciuric hypercalcemia type 1 [ORDO Disease]
- familial hyperparathyroidism [SNOMED Notion]
- familial hypocalciuric hypercalcemia [DO Concept]
MeSH term(s) associated for indexing
- hypercalcemia [MeSH Descriptor]
ORDO relation(s)
- Familial hypocalciuric hypercalcemia type 1 [ORDO Disease]
Record concept(s)
- Hypocalciuric hypercalcemia, familial, type 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hypocalciuric hypercalcemia type 1 [ORDO Disease]
- Hypocalciuric hypercalcemia, familial, type I [OMIM Phenotype]
Validated automatic mappings to NTBT
- calcium metabolism disorder [Disease (Nov.)]
- familial hypocalciuric hypercalcemia [Disease (Nov.)]

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