Sturge–Weber syndrome (Q1886238)

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neurological and skin disorder associated with port-wine stains of the face, glaucoma, seizures, intellectual disability, and cerebral malformations
  • encephalotrigeminal angiomatosis
  • Sturge-Weber-Krabbe disease
  • Sturge-Weber syndrome
  • Sturge-Weber Syndrome
  • Sturge-Weber-Krabbe syndrome
  • SWS type II - Facial angioma alone, no CNS involvement
  • SWS type III - Isolated leptomeningeal angiomas
  • Sturge-Weber-Krabbe angiomatosis
  • Sturge-Weber Disease
  • Meningeal capillary angiomatosis
  • Leptomeningeal angiomatosis
  • Encephalofacial angiomatosis
  • Sturge-Weber-Dimitri syndrome
  • Sturge Weber syndrome
  • STURGE-WEBER SYNDROME; SWS
  • SWS
  • Encephalotrigeminal Syndrome
  • SWS type I - Facial and leptomeningeal angiomas
  • Fourth phacomatosis
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English
Sturge–Weber syndrome
neurological and skin disorder associated with port-wine stains of the face, glaucoma, seizures, intellectual disability, and cerebral malformations
  • encephalotrigeminal angiomatosis
  • Sturge-Weber-Krabbe disease
  • Sturge-Weber syndrome
  • Sturge-Weber Syndrome
  • Sturge-Weber-Krabbe syndrome
  • SWS type II - Facial angioma alone, no CNS involvement
  • SWS type III - Isolated leptomeningeal angiomas
  • Sturge-Weber-Krabbe angiomatosis
  • Sturge-Weber Disease
  • Meningeal capillary angiomatosis
  • Leptomeningeal angiomatosis
  • Encephalofacial angiomatosis
  • Sturge-Weber-Dimitri syndrome
  • Sturge Weber syndrome
  • STURGE-WEBER SYNDROME; SWS
  • SWS
  • Encephalotrigeminal Syndrome
  • SWS type I - Facial and leptomeningeal angiomas
  • Fourth phacomatosis

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Sturge–Weber syndrome
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