Preferred Name | Purine-Pyrimidine Metabolism, Inborn Errors [Disease/Finding] | |
Synonyms |
Purine-Pyrimidine Metabolism, Inborn Errors Purine Pyrimidine Metabolism, Inborn Errors |
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ID |
http://purl.bioontology.org/ontology/NDFRT/N0000002552 |
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altLabel |
Purine-Pyrimidine Metabolism, Inborn Errors Purine Pyrimidine Metabolism, Inborn Errors |
|
cui |
C0034139 |
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MESH DEFINITION |
Dysfunctions in the metabolism of PURINES or PYRIMIDINES resulting from inborn genetic mutations that are inherited or acquired in utero. |
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MESH DUI |
D011686 |
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MeSH name |
Purine-Pyrimidine Metabolism, Inborn Errors |
|
MESH UI |
M0018168 |
|
NDFRT kind |
DISEASE_KIND |
|
notation |
N0000002552 |
|
NUI |
N0000002552 |
|
prefLabel |
Purine-Pyrimidine Metabolism, Inborn Errors [Disease/Finding] |
|
SNOMED CID |
238006008 |
|
tui |
T047 |
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subClassOf |
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