Preferred Name |
Machado-Joseph Disease |
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Synonyms |
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ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Machado-Joseph_Disease |
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DEFINITION |
A very rare, autosomal dominant inherited neurodegenerative disorder. Signs and symptoms include ataxia, spasticity, and abnormalities in the ocular movements. |
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FULL_SYN |
Spinocerebellar Ataxia Type 3 |
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isDefinedBy |
A very rare, autosomal dominant inherited neurodegenerative disorder. Signs and symptoms include ataxia, spasticity, and abnormalities in the ocular movements. |
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label |
Machado-Joseph Disease |
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prefixIRI |
Thesaurus:Machado-Joseph_Disease |
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prefLabel |
Machado-Joseph Disease |
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Synonym |
Spinocerebellar Ataxia Type 3 |
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subClassOf |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Rare_Non-Neoplastic_Disorder http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Spinocerebellar_Ataxia |
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