Ferritin light chain

Preferred Label : Ferritin light chain;

Symbol : FTL;

CISMeF acronym : FTL;

Type : Gene;

Ensembl ID : ENSG00000087086;

Prefixed ID : *134790;

Details

Origin ID

134790;

UMLS CUI

C1414852;

Automatic exact mappings (from CISMeF team)
- Ferritin Light Chain Measurement [NCIt concept]
- apoferritins [MeSH Descriptor]
- ferritin light chain [ORDO Gene]
- ferritin light chain [HGNC gene]
- ferritin light chain [MeSH concept]
HGNC gene
- ferritin light chain [HGNC gene]
ORDO concept(s)
- ferritin light chain [ORDO Gene]
Phenotypes related
- Hyperferritinemia with or without cataract [OMIM Phenotype]
- L-ferritin deficiency [OMIM Phenotype]
- Neurodegeneration with brain iron accumulation 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ferritin light chain [HGNC gene]

Keyword's position in hierarchy(ies) :

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