About: Romano-Ward Syndrome     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • Romano-Ward Syndrome
rdfs:subClassOf
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Romano-Ward Syndrome
UMLS_CUI
  • C0035828
FULL_SYN
  • Romano-Ward SyndromePTNCI
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.NCI
code
  • C85049
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