orotic aciduria (Q21836): Difference between revisions
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Created claim: subclass of (P1): pyrimidine metabolic disorder (Q21837) |
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| Property / subclass of | |||
| Property / subclass of: vitamin B12- and folate-independent constitutional megaloblastic anemia / rank | |||
Normal rank | |||
Revision as of 21:08, 6 April 2024
pyrimidine metabolic disorder that is characterized by an excessive secretion of orotic acid in urine
- hereditary orotic aciduria
- OROTIC ACIDURIA
- Ump Synthase Deficiency
- Uridine Monophosphate Synthase Deficiency
- Oroticaciduria
- Orotate Phosphoribosyltransferase and Orotidylic Decarboxylase Deficiency
- Uridine monophosphate synthetase deficiency
- Oprt and Odc Deficiency
- Orotic Aciduria Without Megaloblastic Anemia
- Orotic Aciduria 1
- Orotidylic Pyrophosphorylase and Orotidylic Decarboxylase Deficiency
- Orotidylic decarboxylase deficiency
- Umps Deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | orotic aciduria |
pyrimidine metabolic disorder that is characterized by an excessive secretion of orotic acid in urine |
|