Preferred Name | phenylketonuria | |
Synonyms |
PKU maternal phenylketonuria Folling's disease phenylalaninemia |
|
Definitions |
An amino acid metabolic disorder that is characterized by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional. OMIM mapping confirmed by DO. [SN]. |
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ID |
http://purl.obolibrary.org/obo/DOID_9281 |
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comment |
OMIM mapping confirmed by DO. [SN]. |
|
database_cross_reference |
MESH:D010661 UMLS_CUI:C0031485 OMIM:261600 UMLS_CUI:C0085547 ICD9CM:270.1 MESH:D017042 SNOMEDCT_US_2020_03_01:154735006 SNOMEDCT_US_2020_03_01:297225000 GARD:7383 NCI:C81315 ORDO:716 |
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has exact synonym |
PKU maternal phenylketonuria Folling's disease phenylalaninemia |
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has_alternative_id |
DOID:14455 |
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has_obo_namespace |
disease_ontology |
|
id |
DOID:9281 |
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imported from | ||
in_subset | ||
label |
phenylketonuria |
|
notation |
DOID:9281 |
|
prefLabel |
phenylketonuria |
|
textual definition |
An amino acid metabolic disorder that is characterized by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional. |
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subClassOf |