SH2 domain containing 1A

Preferred Label : SH2 domain containing 1A;

Approved symbol HGNC : SH2D1A;

Name synonyms HGNC : Duncan's disease;

Alias symbols HGNC : XLPD; SAP; DSHP; MTCP1; EBVS; XLP;

Chromosome HGNC : Xq25;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000183918;

Details

Origin ID

HGNC:10820;

UMLS CUI

C1420017;

Automatic exact mappings (from CISMeF team)
- Duncan disease [PASCAL descriptor]
- Lymphoproliferative syndrome, X-linked, 1 [OMIM Phenotype]
- Mature t-cell proliferation 1 [OMIM gene]
- SH2 domain containing 1A [ORDO Gene]
- Sh2 domain protein 1a [OMIM gene]
- X-linked lymphoproliferative disease [ORDO Disease]
- lymphoproliferative disorders [MeSH Descriptor]
NCIt concept
- SH2D1A Gene [NCIt concept]
OMIM gene
- Sh2 domain protein 1a [OMIM gene]
Orphanet gene
- SH2 domain containing 1A [ORDO Gene]
See also inter- (CISMeF)
- X-Linked Lymphoproliferative Syndrome [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SH2D1A Gene [NCIt concept]
- SH2D1A gene [LOINC component]
- Sh2 domain protein 1a [OMIM gene]

Keyword's position in hierarchy(ies) :

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