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BioAssay Ontology
Last uploaded:
February 21, 2024
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| Preferred Name | maple syrup urine disease | |
| Synonyms |
dihydrolipoamide dehydrogenase deficiency Ketoacidaemia branched chain ketoaciduria |
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| Definitions |
An organic acidemia that is caused by a deficiency of decarboxylase leading to high concentrations of valine, leucine, isoleucine, and alloisoleucine in the blood, urine, and cerebrospinal fluid and characterized by an odor of maple syrup to the urine, vomiting, hypertonicity, severe mental retardation, seizures, and eventually death unless the condition is treated with dietary measures. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
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| ID |
http://purl.obolibrary.org/obo/DOID_9269 |
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| comment |
Xref MGI.
OMIM mapping confirmed by DO. [SN].
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| database_cross_reference |
OMIM:246900 UMLS_CUI:C0024776 SNOMEDCT_US_2020_03_01:27718001 OMIM:248600 MESH:D008375 ICD10CM:E71.0 OMIM:615135 GARD:3228 NCI:C34806 ORDO:511
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| has exact synonym |
Ketoacidaemia branched chain ketoaciduria
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| has_obo_namespace |
disease_ontology
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| has_related_synonym |
dihydrolipoamide dehydrogenase deficiency dihydrolipoamide dehydrogenase deficiency
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| id |
DOID:9269
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| imported from | ||
| in_subset | ||
| label |
maple syrup urine disease
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| notation |
DOID:9269
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| prefLabel |
maple syrup urine disease
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| textual definition |
An organic acidemia that is caused by a deficiency of decarboxylase leading to high concentrations of valine, leucine, isoleucine, and alloisoleucine in the blood, urine, and cerebrospinal fluid and characterized by an odor of maple syrup to the urine, vomiting, hypertonicity, severe mental retardation, seizures, and eventually death unless the condition is treated with dietary measures.
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| subClassOf |
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