| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A glucose metabolism disorder that is characterized by chronic haemolytic anaemia, cardiomyopathy, susceptibility to infections and severe neurological dysfunction, and has_physical_basis_in the triosephosphate isomerase enzyme (TPI1) gene inherited as an autosomal recessive trait. (Human Disease Ontology, DOID_0050884) |
| External Link | https://www.disgenet.org/browser/0/1/0/C1860808 |
| Similar Terms | |
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1 genes associated with the disease Triosephosphate Isomerase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| TPI1 | triosephosphate isomerase 1 |
