Link to this page
Pediatric Terminology
Last uploaded:
January 25, 2013
Jump to:
| Preferred Name | Maple_Syrup_Urine_Disease | |
| Synonyms |
|
|
| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Maple_Syrup_Urine_Disease |
|
| ID |
C34806
|
|
| NCI_Definition |
An autosomal recessive inherited disorder caused by mutations in the BCKDHA, BCKDHB, DBT, and DLD genes. It is characterized by a deficiency of branched-chain alpha-keto acid dehydrogenase complex, leading to accumulation of metabolites in the body fluids. The name of the disease derives from the sweet odor of the urine in infants, reminiscent of maple syrup. Signs and symptoms usually appear in infancy and include lethargy and developmental delays. If untreated, it may lead to seizures, coma, and death.
|
|
| NCI_PT |
Maple Syrup Urine Disease
|
|
| NICHD_Definition |
_
|
|
| prefixIRI |
Maple_Syrup_Urine_Disease
|
|
| prefLabel |
Maple_Syrup_Urine_Disease
|
|
| Subset_Association1 |
NICHD Pediatric Terminology
|
|
| Subset_Association2 |
Neonatal Research Network Terminology
|
|
| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Autosomal_Recessive_Hereditary_Disorder |
Add comment
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |
Create mapping