Plexin d1 - CISMeF

Preferred Label : Plexin d1;

Symbol : PLXND1;

CISMeF acronym : PLXND1;

Type : Gene;

Ensembl ID : ENSG00000004399;

Prefixed ID : *604282;

Details

Origin ID

604282;

UMLS CUI

C1418668;

Automatic exact mappings (from CISMeF team)
- PLXND1 Gene [NCIt concept]
- Plexin-D1 [NCIt concept]
- plexin D1 [ORDO Gene]
- plexin D1 [HGNC gene]
HGNC gene
- plexin D1 [HGNC gene]
NCIt concept(s)
- PLXND1 Gene [NCIt concept]
- PLXND1 wt Allele [NCIt concept]
- Plexin-D1 [NCIt concept]
ORDO concept(s)
- plexin D1 [ORDO Gene]
Phenotypes related
- Congenital heart defects, multiple types, 9 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PLXND1 Gene [NCIt concept]
- plexin D1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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