synaptophysin - CISMeF

Preferred Label : synaptophysin;

Approved symbol HGNC : SYP;

Alias symbols HGNC : MRX96;

Chromosome HGNC : Xp11.23;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000102003;

Details

Origin ID

HGNC:11506;

UMLS CUI

C1420554;

Automatic exact mappings (from CISMeF team)
- Intellectual developmental disorder, X-linked 96 [OMIM Phenotype]
- Synaptophysin [OMIM gene]
- Synaptophysin [LOINC component]
- Synaptophysin [NCIt concept]
- synaptophysin [ORDO Gene]
- synaptophysin [MeSH concept]
- synaptophysin [MeSH Descriptor]
NCIt concept
- SYP Gene [NCIt concept]
OMIM gene
- Synaptophysin [OMIM gene]
Orphanet gene
- synaptophysin [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SYP Gene [NCIt concept]
- Synaptophysin [OMIM gene]

Keyword's position in hierarchy(ies) :

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