Spastin - CISMeF

Preferred Label : Spastin;

Symbol : SPAST;

CISMeF acronym : SPAST;

Type : Gene;

Alternative titles and symbols : Spg4 gene; SPG4;

Ensembl ID : ENSG00000021574;

Prefixed ID : *604277;

Details

Origin ID

604277;

UMLS CUI

C1539809;

Automatic exact mappings (from CISMeF team)
- Autosomal dominant spastic paraplegia type 4 [ORDO Disease]
- SPAST gene [LOINC component]
- Spastin [MeSH Descriptor]
- hereditary spastic paraplegia 4 [DO Concept]
- spastin [ORDO Gene]
- spastin [HGNC gene]
HGNC gene
- spastin [HGNC gene]
NCIt concept(s)
- SPAST Gene [NCIt concept]
- SPAST wt Allele [NCIt concept]
- Spastin [NCIt concept]
ORDO concept(s)
- spastin [ORDO Gene]
Phenotypes related
- Spastic paraplegia 4, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SPAST gene [LOINC component]
- spastin [HGNC gene]

Keyword's position in hierarchy(ies) :

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