Triosephosphate isomerase 1

Preferred Label : Triosephosphate isomerase 1;

Obsolete resource : true;

Alternative titles and symbols : Tpi1; Tpitriosephosphate isomerase deficiency;

Inheritance : Autosomal dominant (12p13);

Details

Origin ID

190450;

UMLS CUI

C1420871;

Automatic exact mappings (from CISMeF team)
- TPI1 Gene [NCIt concept]
Currated CISMeF NLP mapping
- Triose phosphate isomerase deficiency (disorder) [SNOMED CT concept]
- Triose phosphate-isomerase deficiency [ORDO Disease]
- Triosephosphate Isomerase Deficiency [NCIt concept]
- triosephosphate isomerase 1 [ORDO Gene]
- triosephosphate isomerase deficiency [DO Concept]
- triosephosphate isomerase deficiency [MeSH Supplementary Concept]
- triosephosphate isomerase deficiency [MeSH concept]
Matching ORDO disease(s)
- Triose phosphate-isomerase deficiency [ORDO Disease]
NCIt concept(s)
- TPI1 Gene [NCIt concept]
- TPI1 wt Allele [NCIt concept]
- Triosephosphate Isomerase [NCIt concept]
ORDO concept(s)
- triosephosphate isomerase 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- TPI1 Gene [NCIt concept]
- triosephosphate isomerase 1 [ORDO Gene]
- triosephosphate isomerase 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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