prosaposin - CISMeF

Preferred Label : prosaposin;

Approved symbol HGNC : PSAP;

Name synonyms HGNC : saposin-A; precursor of saposins; variant Gaucher disease and variant metachromatic leukodystrophy; saposin-C; saposin-B; saposin-D;

Chromosome HGNC : 10q22.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000197746;

Details

Origin ID

HGNC:9498;

UMLS CUI

C1418975;

Automatic exact mappings (from CISMeF team)
- Prosaposin [OMIM gene]
- Prosaposin [NCIt concept]
- Saposin-A [NCIt concept]
- Saposin-B [NCIt concept]
- Saposin-C [NCIt concept]
- Saposin-D [NCIt concept]
- prosaposin [ORDO Gene]
NCIt concept
- PSAP Gene [NCIt concept]
OMIM gene
- Prosaposin [OMIM gene]
Orphanet gene
- prosaposin [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PSAP Gene [NCIt concept]
- PSAP gene [LOINC component]
- Prosaposin [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients