endoglin - CISMeF

Preferred Label : endoglin;

Approved symbol HGNC : ENG;

Alias symbols HGNC : END; CD105; HHT1;

Chromosome HGNC : 9q34.11;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000106991;

Details

Origin ID

HGNC:3349;

UMLS CUI

C1366583;

Automatic exact mappings (from CISMeF team)
- Endoglin [OMIM gene]
- Endoglin [MeSH Descriptor]
- Endoglin [MeSH concept]
- Telangiectasia, hereditary hemorrhagic, type 1 [OMIM Phenotype]
- endoglin [ORDO Gene]
- transforming growth factor beta receptor activity, type III [GO term]
NCIt concept
- ENG Gene [NCIt concept]
OMIM gene
- Endoglin [OMIM gene]
Orphanet gene
- endoglin [ORDO Gene]
See also inter- (CISMeF)
- Endoglin [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ENG Gene [NCIt concept]
- ENG gene [LOINC component]
- Endoglin [OMIM gene]

Keyword's position in hierarchy(ies) :

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