Preferred Name |
Amino_Acid_Metabolism_Disorder |
|
Synonyms |
|
|
ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Amino_Acid_Metabolism_Disorder |
|
ID |
C97090 |
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NCI_Definition |
An inherited disorder that affects the metabolism of the amino acids. Representative examples include alkaptonuria, homocystinuria, tyrosinemia, and phenylketonuria. |
|
NCI_PT |
Amino Acid Metabolism Disorder |
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NICHD_Definition |
_ |
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prefixIRI |
Amino_Acid_Metabolism_Disorder |
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prefLabel |
Amino_Acid_Metabolism_Disorder |
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Subset_Association1 |
NICHD Pediatric Terminology |
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Subset_Association2 |
Neonatal Research Network Terminology |
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SYN |
Disorder of Amino Acid Metabolism |
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subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Metabolic_Disorder |
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