R-spondin 2 - CISMeF

Preferred Label : R-spondin 2;

Symbol : RSPO2;

CISMeF acronym : RSPO2;

Type : Gene;

Alternative titles and symbols : R-spondin family, member 2; CRISTIN2;

Ensembl ID : ENSG00000147655;

Prefixed ID : *610575;

Details

Origin ID

610575;

UMLS CUI

C1826945;

Automatic exact mappings (from CISMeF team)
- R-spondin 2 [ORDO Gene]
- R-spondin 2 [HGNC gene]
- RSPO2 Gene [NCIt concept]
- RSPO2 wt Allele [NCIt concept]
HGNC gene
- R-spondin 2 [HGNC gene]
NCIt concept(s)
- R-Spondin-2 [NCIt concept]
- RSPO2 Gene [NCIt concept]
- RSPO2 wt Allele [NCIt concept]
ORDO concept(s)
- R-spondin 2 [ORDO Gene]
Phenotypes related
- Humerofemoral hypoplasia with radiotibial ray deficiency [OMIM Phenotype]
- Tetraamelia syndrome 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- R-spondin 2 [HGNC gene]
- RSPO2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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