hypercalciuria, absorptive, 2

Preferred Label : hypercalciuria, absorptive, 2;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0563090;

UMLS CUI

C0342639;

Automatic exact mappings (from CISMeF team)
- Hypercalciuria [ICD-11 Subcategory]
- adenylate cyclase 10 [ORDO Gene]
Currated CISMeF NLP mapping
- Disorders of calcium metabolism [ICD-10 Sub-category]
- Disorders of calcium metabolism [ICD-10 Sub-category (who)]
- Hypercalciuria, absorptive, 2 [OMIM Phenotype]
- Idiopathic hypercalciuria [MedDRA LLT]
- Idiopathic hypercalciuria [ORDO Disease]
Related record
- hypercalciuria, absorptive, 2 [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Familial idiopathic hypercalciuria (disorder) [SNOMED CT concept]
- Hypercalciuria, absorptive, 2 [OMIM Phenotype]
Validated automatic mappings to NTBT
- calcium metabolism disorder [Disease (Nov.)]