Synaptotagmin 2

Preferred Label : Synaptotagmin 2;

Symbol : SYT2;

CISMeF acronym : SYT2;

Type : Gene;

Ensembl ID : ENSG00000143858;

Prefixed ID : *600104;

Details

Origin ID

600104;

UMLS CUI

C1420557;

Automatic exact mappings (from CISMeF team)
- synaptotagmin 2 [ORDO Gene]
- synaptotagmin 2 [HGNC gene]
- synaptotagmin ii [MeSH Descriptor]
HGNC gene
- synaptotagmin 2 [HGNC gene]
ORDO concept(s)
- synaptotagmin 2 [ORDO Gene]
Phenotypes related
- Myasthenic syndrome, congenital, 7a, presynaptic, and distal motor neuropathy, autosomal dominant [OMIM Phenotype]
- Myasthenic syndrome, congenital, 7b, presynaptic, autosomal recessive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- synaptotagmin 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients