Lp(A) deficiency, congenital

Preferred Label : Lp(A) deficiency, congenital;

MeSH synonym : Lipoprotein(A) deficiency, congenital;

Origin ID

C563618;

UMLS CUI

C1835362;

Automatic exact mappings (from CISMeF team)
- Apolipoprotein(a) [OMIM Phenotype]
Currated CISMeF NLP mapping
- Lipoprotein(a) quantitative trait locus [OMIM Phenotype]
MeSH term(s) associated for indexing
- lipid metabolism, inborn errors [MeSH Descriptor]
- lipoprotein(a) [MeSH Descriptor]
Record concept(s)
- Lp(A) deficiency, congenital [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]