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Cigarette Smoke Exposure Ontology
Last uploaded:
July 10, 2014
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| Id | http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Homocystinuria
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Homocystinuria
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| Preferred Name | Homocystinuria |
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| label |
Homocystinuria
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| prefLabel |
Homocystinuria
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| DEFINITION |
An autosomal recessive inherited metabolic disorder caused by mutations in the CBS, MTHFR, MTR, and MTRR genes. It is characterized by abnormalities in the methionine metabolism and is associated with deficiency of cystathionine synthase. It results in the accumulation of homocysteine in the serum. It may affect the cardiovascular, musculoskeletal and the central nervous systems.
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| isDefinedBy |
An autosomal recessive inherited metabolic disorder caused by mutations in the CBS, MTHFR, MTR, and MTRR genes. It is characterized by abnormalities in the methionine metabolism and is associated with deficiency of cystathionine synthase. It results in the accumulation of homocysteine in the serum. It may affect the cardiovascular, musculoskeletal and the central nervous systems.
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| prefixIRI |
Thesaurus:Homocystinuria
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| subClassOf | |
| type |
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