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loading...| Preferred Name |
Amino Acid Metabolism Disorder |
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| Synonyms |
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| Definitions |
An inherited disorder that affects the metabolism of the amino acids. Representative examples include alkaptonuria, homocystinuria, tyrosinemia, and phenylketonuria. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C97090 |
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| code |
C97090 |
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| Contributing_Source |
NICHD |
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| definition |
An inherited disorder that affects the metabolism of the amino acids. Representative examples include alkaptonuria, homocystinuria, tyrosinemia, and phenylketonuria. |
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| in_subset | ||
| label |
Amino Acid Metabolism Disorder |
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| Preferred_Name |
Amino Acid Metabolism Disorder |
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| prefixIRI |
NCIT:C97090 |
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| prefLabel |
Amino Acid Metabolism Disorder |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0002514 |
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| subClassOf |
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