Fibrillin 2 - CISMeF

Preferred Label : Fibrillin 2;

Symbol : FBN2;

CISMeF acronym : FBN2;

Type : Gene;

Ensembl ID : ENSG00000138829;

Prefixed ID : *612570;

Details

Origin ID

612570;

UMLS CUI

C1414543;

Automatic exact mappings (from CISMeF team)
- FBN2 Gene [NCIt concept]
- FBN2 gene [LOINC component]
- Fibrillin-2 [NCIt concept]
- Fibrillin-2 [MeSH Descriptor]
- fibrillin 2 [ORDO Gene]
- fibrillin 2 [HGNC gene]
HGNC gene
- fibrillin 2 [HGNC gene]
NCIt concept(s)
- FBN2 Gene [NCIt concept]
- FBN2 wt Allele [NCIt concept]
- Fibrillin-2 [NCIt concept]
ORDO concept(s)
- fibrillin 2 [ORDO Gene]
Phenotypes related
- Contractural arachnodactyly, congenital [OMIM Phenotype]
- Macular degeneration, early-onset [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FBN2 Gene [NCIt concept]
- FBN2 gene [LOINC component]
- fibrillin 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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