Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
triosephosphate isomerase deficiency
Summary
- Synonym
-
- Triose phosphate-isomerase deficiency
- Definition
- A glucose metabolism disorder that is characterized by chronic haemolytic anaemia, cardiomyopathy, susceptibility to infections and severe neurological dysfunction, and has_material_basis_in the triosephosphate isomerase enzyme (TPI1) gene inherited as an autosomal recessive trait.
- Super Class
- glucose metabolism disease
External Links
- Disease Ontology
- DOID:0050884
- Mondo Disease Ontology
- MeSH
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001265 | Hyporeflexia |
| HP:0002098 | Respiratory distress |
| HP:0006579 | Prolonged neonatal jaundice |
| HP:0001522 | Death in infancy |
| HP:0001257 | Spasticity |
| HP:0002059 | Cerebral atrophy |
| HP:0000952 | Jaundice |
| HP:0001878 | Hemolytic anemia |
| HP:0002747 | Respiratory insufficiency due to muscle weakness |
| HP:0001324 | Muscle weakness |
