hypomagnesemia 5, renal, with ocular involvement

Preferred Label : hypomagnesemia 5, renal, with ocular involvement;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0565723;

UMLS CUI

C1855466;

Currated CISMeF NLP mapping
- Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) [SNOMED CT concept]
- Hypomagnesemia 5, renal, with or without ocular involvement [OMIM Phenotype]
- Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement [ORDO Disease]
- renal hypomagnesemia 5 [Disease (Nov.)]
- renal hypomagnesemia 5 with ocular involvement [DO Concept]
Related record
- hypomagnesemia 5, renal, with ocular involvement [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) [SNOMED CT concept]
- Hypomagnesemia 5, renal, with or without ocular involvement [OMIM Phenotype]
- renal hypomagnesemia 5 [Disease (Nov.)]