Titin - CISMeF

Preferred Label : Titin;

Symbol : TTN;

CISMeF acronym : TTN;

Type : Gene;

Alternative titles and symbols : CONNECTIN;

Ensembl ID : ENSG00000155657;

Prefixed ID : *188840;

Détails

Origin ID

188840;

UMLS CUI

C1421222;

Automatic exact mappings (from CISMeF team)
- TTN Gene [NCIt concept]
- Titin [FMA entity]
- Titin [NCIt concept]
- Titin [LOINC component]
- Transient Tachypnea of the Newborn [NCIt concept]
- Transient tachypnoea of newborn [ICD-11 Subcategory]
- connectin [MeSH concept]
- connectin [MeSH Descriptor]
- titin [ORDO Gene]
- titin [HGNC gene]
HGNC gene
- titin [HGNC gene]
NCIt concept(s)
- TTN Gene [NCIt concept]
- TTN wt Allele [NCIt concept]
- Titin [NCIt concept]
ORDO concept(s)
- titin [ORDO Gene]
Phenotypes related
- Cardiomyopathy, dilated, 1g [OMIM Phenotype]
- Cardiomyopathy, familial hypertrophic, 9 [OMIM Phenotype]
- Congenital myopathy 5 with cardiomyopathy [OMIM Phenotype]
- Muscular dystrophy, limb-girdle, autosomal recessive 10 [OMIM Phenotype]
- Myopathy, myofibrillar, 9, with early respiratory failure [OMIM Phenotype]
- Tibial muscular dystrophy, tardive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- TTN Gene [NCIt concept]
- titin [HGNC gene]

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