hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial

Preferred Label : hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial;

Origin ID

C564024;

UMLS CUI

C1839021;

Currated CISMeF NLP mapping
- Hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial [OMIM Phenotype]
MeSH term(s) associated for indexing
- hypercholesterolemia [MeSH Descriptor]
- hypertension [MeSH Descriptor]
- renal tubular transport, inborn errors [MeSH Descriptor]
Record concept(s)
- hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial [OMIM Phenotype]