Uraciluria
Symptom Information:
| Symptom ID: | HPO:0012127 | ||
| Synonyms: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of nucleobase metabolism(HPO:0010932) Abnormality of pyrimidine metabolism(HPO:0004353) Uraciluria(HPO:0012127) MedDRA: |
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| Database Frequency: | 2 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
| Ornithine transcarbamylase deficiency | (Orphanet:664) |