titin - CISMeF

Preferred Label : titin;

Approved symbol HGNC : TTN;

Alias symbols HGNC : FLJ32040; CMPD4; CMH9; LGMD2J; TMD; MYLK5;

Chromosome HGNC : 2q31.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000155657;

Details

Origin ID

HGNC:12403;

UMLS CUI

C1421222;

Automatic exact mappings (from CISMeF team)
- Tibial muscular dystrophy, tardive [OMIM Phenotype]
- Titin [OMIM gene]
- Titin [FMA entity]
- Titin [NCIt concept]
- Titin [LOINC component]
- connectin [MeSH Descriptor]
- titin [ORDO Gene]
NCIt concept
- TTN Gene [NCIt concept]
OMIM gene
- Titin [OMIM gene]
Orphanet gene
- titin [ORDO Gene]
See also inter- (CISMeF)
- Cardiomyopathy, familial hypertrophic, 9 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- TTN Gene [NCIt concept]
- Titin [OMIM gene]

Keyword's position in hierarchy(ies) :

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