hypercholesterolemia, autosomal dominant, 3

Preferred Label : hypercholesterolemia, autosomal dominant, 3;

MeSH note : mutation in PCSK9;

MeSH synonym : HCHOLA3; FH3;

Origin ID

C566337;

UMLS CUI

C1863551;

Currated CISMeF NLP mapping
- Hypercholesterolemia, familial, 3 [OMIM Phenotype]
MeSH term(s) associated for indexing
- hyperlipoproteinemias [MeSH Descriptor]
Record concept(s)
- hypercholesterolemia, autosomal dominant, 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypercholesterolemia, familial, 3 [OMIM Phenotype]