pyrimidine metabolic disorder (Q21837): Difference between revisions
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Created claim: subclass of (P1): inborn errors of purine–pyrimidine metabolism (Q21838) |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_79193 |
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| Property / exact match | |||
| Property / exact match: http://purl.obolibrary.org/obo/DOID_0050832 / rank | |||
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| Property / exact match | |||
| Property / exact match: http://identifiers.org/doid/DOID:0050832 / rank | |||
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| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_79193 / rank | |||
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Latest revision as of 21:02, 6 April 2024
inherited metabolic disorder involving dysfunction of pyrimidine metabolism
- rare inborn error of pyrimidine nucleobase metabolic process
- Disorder of pyrimidine metabolism
- inborn error of pyrimidine nucleobase metabolic process
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | pyrimidine metabolic disorder |
inherited metabolic disorder involving dysfunction of pyrimidine metabolism |
|