Troponin t1, skeletal, slow

Preferred Label : Troponin t1, skeletal, slow;

Symbol : TNNT1;

CISMeF acronym : TNNT1;

Type : Gene;

Alternative titles and symbols : Troponin t;

Ensembl ID : ENSG00000105048;

Prefixed ID : *191041;

Details

Origin ID

191041;

UMLS CUI

C1420827;

Automatic exact mappings (from CISMeF team)
- Troponin T [MedDRA Preferred Term]
- Troponin T [NCIt concept]
- Troponin T (substance) [SNOMED CT concept]
- Troponin T Measurement [NCIt concept]
- troponin T [MeSH concept]
- troponin T1, slow skeletal type [ORDO Gene]
- troponin T1, slow skeletal type [HGNC gene]
- troponin t [SNOMED Notion]
- troponin t [MeSH Descriptor]
HGNC gene
- troponin T1, slow skeletal type [HGNC gene]
ORDO concept(s)
- troponin T1, slow skeletal type [ORDO Gene]
Phenotypes related
- Nemaline myopathy 5a, autosomal recessive, severe infantile [OMIM Phenotype]
- Nemaline myopathy 5b, autosomal recessive, childhood-onset [OMIM Phenotype]
- Nemaline myopathy 5c, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- troponin T1, slow skeletal type [HGNC gene]

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