Perilipin 1 - CISMeF

Preferred Label : Perilipin 1;

Symbol : PLIN1;

CISMeF acronym : PLIN1;

Type : Gene;

Alternative titles and symbols : PLIN;

Ensembl ID : ENSG00000166819;

Prefixed ID : *170290;

Details

Origin ID

170290;

UMLS CUI

C1418649;

Automatic exact mappings (from CISMeF team)
- Perilipin 1 related familial partial lipodystrophy (disorder) [SNOMED CT concept]
- Perilipin-1 [MeSH concept]
- Perilipin-1 [MeSH Descriptor]
- perilipin 1 [ORDO Gene]
- perilipin 1 [HGNC gene]
HGNC gene
- perilipin 1 [HGNC gene]
NCIt concept(s)
- PLIN1 Gene [NCIt concept]
- PLIN1 wt Allele [NCIt concept]
- Perilipin-1 [NCIt concept]
ORDO concept(s)
- perilipin 1 [ORDO Gene]
Phenotypes related
- Lipodystrophy, familial partial, type 4 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PLIN1 Gene [NCIt concept]
- perilipin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients