Preferred Name |
Romano-Ward Syndrome |
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Synonyms |
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ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Romano-Ward_Syndrome |
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DEFINITION |
An autosomal dominant form of long QT syndrome caused by mutations in the KCNE1, KCNE2, KCNH2, KCNQ1, SCN5A, and ANK2 genes. It is manifested with arrhythmias. |
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label |
Romano-Ward Syndrome |
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prefixIRI |
Thesaurus:Romano-Ward_Syndrome |
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prefLabel |
Romano-Ward Syndrome |
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subClassOf |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Long_QT_Syndrome |
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