Spartin - CISMeF

Preferred Label : Spartin;

Symbol : SPART;

CISMeF acronym : SPART;

Type : Gene;

Alternative titles and symbols : SPG20; KIAA0610;

Ensembl ID : ENSG00000133104;

Prefixed ID : *607111;

Details

Origin ID

607111;

UMLS CUI

C1425570;

Automatic exact mappings (from CISMeF team)
- Autosomal recessive spastic paraplegia type 20 [ORDO Disease]
- Troyer syndrome [DO Concept]
- spartin [ORDO Gene]
- spartin [HGNC gene]
HGNC gene
- spartin [HGNC gene]
ORDO concept(s)
- spartin [ORDO Gene]
Phenotypes related
- Spastic paraplegia 20, autosomal recessive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- spartin [HGNC gene]

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