| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Pentosuria is an inborn error of metabolism which is characterized by the excretion of 1 to 4 g of the pentose L-xylulose in the urine per day. (Orphanet Rare Disease Ontology, Orphanet_2843) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C536652 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Pentosuria from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| DCXR | dicarbonyl/L-xylulose reductase | 2.88009 |
