Hypocalciuric hypercalcemia, familial, type 1

Preferred Label : Hypocalciuric hypercalcemia, familial, type 1;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0531606;

UMLS CUI

C0342637;

Automatic exact mappings (from CISMeF team)
- Familial hypocalciuric hypercalcemia [MedDRA LLT]
- Familial hypocalciuric hypercalcemia (disorder) [SNOMED CT concept]
- Hypocalciuric hypercalcemia, familial, type I [OMIM Phenotype]
Currated CISMeF NLP mapping
- Familial hypocalciuric hypercalcemia type 1 [ORDO Disease]
Related record
- hypocalciuric hypercalcemia, familial, type 1 [MeSH Supplementary 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]