Apolipoprotein(a)

Preferred Label : Apolipoprotein(a);

Symbol : LPA;

CISMeF acronym : LPA; SPB;

Type : Gene and phenotype, combined;

Included titles and symbols : Lipoprotein(a); Lipoprotein types--lp system lp(a) hyperlipoproteinemia; Sinking pre-beta-lipoprotein; Lipoprotein(a) deficiency, congenital; Lp(a) deficiency, congenital; Coronary artery disease, susceptibility to; Lp(a); SPB;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutations in the apolipoprotein lp(a) gene (lpa, 152200.0001);

Laboratory abnormalities : Elevated plasma levels of lp(a);

Prefixed ID : 152200;

Details

Origin ID

152200;

UMLS CUI

C1439335;

Automatic exact mappings (from CISMeF team)
- Apolipoprotein [MedDRA Preferred Term]
- Apolipoprotein (a) (substance) [SNOMED CT concept]
- Apolipoprotein (substance) [SNOMED CT concept]
- Apolipoprotein A [NCIt concept]
- Apolipoprotein A [LOINC component]
- Apolipoprotein A (substance) [SNOMED CT concept]
- Apolipoprotein A Measurement [NCIt concept]
- Apolipoprotein(a) [NCIt concept]
- LPA Gene [NCIt concept]
- LPA gene [LOINC component]
- Lepidic Adenocarcinoma [NCIt concept]
- Line Probe Assay [NCIt concept]
- Lipoprotein [FMA entity]
- Lipoprotein [NCIt concept]
- Lipoprotein (a) [MedDRA Preferred Term]
- Lipoprotein (a) (substance) [SNOMED CT concept]
- Lipoprotein (substance) [SNOMED CT concept]
- Lipoprotein a [LOINC component]
- Lipoprotein a Measurement [NCIt concept]
- Lipoproteins [EDAM topic]
- Logopenic progressive aphasia [ORDO Disease]
- Lp(A) deficiency, congenital [MeSH concept]
- Lp(A) deficiency, congenital [MeSH Supplementary Concept]
- Solitary Plasmacytoma of Bone [NCIt concept]
- apolipoprotein a [SNOMED Notion]
- apolipoproteins [MeSH Descriptor]
- apolipoproteins [MeSH concept]
- apolipoproteins A [MeSH concept]
- apolipoproteins a [MeSH Descriptor]
- apoprotein(a) [MeSH Descriptor]
- apoprotein(a) [MeSH concept]
- lipid transporter activity [GO term]
- lipoprotein (a-) [MeSH concept]
- lipoprotein Types--Lp system Lp(A) hyperlipoproteinemia [MeSH concept]
- lipoprotein Types--Lp system Lp(A) hyperlipoproteinemia [MeSH Supplementary Concept]
- lipoprotein(a) [MeSH Descriptor]
- lipoprotein(a) [HGNC gene]
- lipoprotein(a) [MeSH concept]
- lipoproteins [IUPAC Term]
- lipoproteins [MeSH concept]
- lipoproteins [MeSH Descriptor]
- spindle pole body [GO term]
NCIt concept(s)
- Apolipoprotein(a) [NCIt concept]
- LPA Gene [NCIt concept]
- LPA wt Allele [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- LPA Gene [NCIt concept]
- LPA gene [LOINC component]
- Lipoprotein (a) (substance) [SNOMED CT concept]
- Lipoprotein a [LOINC component]
- lipoprotein(a) [HGNC gene]
- lipoprotein(a) [MeSH concept]
- lipoprotein(a) [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

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