Search Ontology:
Human Disease
pentosuria
- Term ID
- DOID:0111258
- Synonyms
-
- essential pentosuria
- L-xylulose reductase deficiency
- L-xylulosuria
- PNTSU
- xylitol dehydrogenase deficiency
- Definition
- An amino acid metabolic disorder characterized by excretion of excess pentose L-xylulose (1-4 g/day) in the urine that has_material_basis_in homozygous or compound heterozygous mutation in DCXR on 17q25.3. https://www.ncbi.nlm.nih.gov/pubmed/22042873
- References
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- GARD:418
- ICD10CM:E74.89
- MEDDRA:10064170
- MESH:C536652
- MIM:260800
- ORDO:2843
- SNOMEDCT_US_2023_03_01:190764000
- UMLS_CUI:C0268162
- Ontology
- Human Disease ( DOID:0111258 )
- is a type of
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Genes Involved
Zebrafish Models