Apolipoprotein b

Preferred Label : Apolipoprotein b;

Symbol : APOB;

CISMeF acronym : APOB;

Type : Gene;

Included titles and symbols : Apob100; Apob48; Apolipoprotein b allotypes; Ag lipoprotein types;

Description : Apolipoprotein B is the main apolipoprotein on chylomicrons and low density lipoproteins (LDLs). It occurs in the plasma in 2 main forms, apoB48 and apoB100. The first is synthesized exclusively by the intestine, the second by the liver (summary by Law et al., 1985).;

Ensembl ID : ENSG00000084674;

Prefixed ID : *107730;

Détails

Origin ID

107730;

UMLS CUI

C1412471;

Automatic exact mappings (from CISMeF team)
- APOB Gene [NCIt concept]
- APOB gene [LOINC component]
- Apo-B [MedDRA LLT]
- Apolipoprotein B Measurement [NCIt concept]
- Apolipoprotein B-100 [NCIt concept]
- Apolipoprotein B100 Measurement [NCIt concept]
- Apolipoprotein B48 Measurement [NCIt concept]
- apolipoprotein B [HGNC gene]
- apolipoprotein b [EMDN type]
- apolipoprotein b-100 [MeSH Descriptor]
- apolipoprotein b-48 [MeSH Descriptor]
Currated CISMeF NLP mapping
- Apolipoprotein B [LOINC component]
- Apolipoprotein B [MedDRA Preferred Term]
- Apolipoprotein B (substance) [SNOMED CT concept]
- apolipoprotein B [ORDO Gene]
- apolipoprotein b [SNOMED Notion]
- apolipoproteins B [MeSH concept]
- apolipoproteins b [MeSH Descriptor]
HGNC gene
- apolipoprotein B [HGNC gene]
NCIt concept(s)
- APOB Gene [NCIt concept]
- APOB wt Allele [NCIt concept]
- Apolipoprotein B-100 [NCIt concept]
ORDO concept(s)
- apolipoprotein B [ORDO Gene]
Phenotypes related
- Hypercholesterolemia, familial, 2 [OMIM Phenotype]
- Hypobetalipoproteinemia, familial, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- APOB Gene [NCIt concept]
- APOB gene [LOINC component]
- Apolipoprotein B (including Ag(x) antigen) gene (substance) [SNOMED CT concept]
- apolipoprotein B [ORDO Gene]
- apolipoprotein B [HGNC gene]

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