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Nervous System Diseases > Neurocutaneous Syndromes > Sturge-Weber Syndrome
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Ectodermal Dysplasia > Neurocutaneous Syndromes > Sturge-Weber Syndrome
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ectodermal Dysplasia > Neurocutaneous Syndromes > Sturge-Weber Syndrome
... > Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ectodermal Dysplasia > Neurocutaneous Syndromes > Sturge-Weber Syndrome
... > Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ectodermal Dysplasia > Neurocutaneous Syndromes > Sturge-Weber Syndrome
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ectodermal Dysplasia > Neurocutaneous Syndromes > Sturge-Weber Syndrome
Neoplasms > Neoplasms by Histologic Type > Neoplasms, Vascular Tissue > Hemangioma > Sturge-Weber Syndrome
Cardiovascular Diseases > Vascular Diseases > Angiomatosis > Sturge-Weber Syndrome

Preferred term

Sturge-Weber Syndrome  

Type

  • mesh:Descriptor

Definition

  • A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects.

Broader concept

Entry terms

  • Angiomatosis Oculoorbital-Thalamic Syndrome
  • Encephalofacial Hemangiomatosis Syndrome
  • Meningofacial Angiomatosis-Cerebral Calcification Syndrome
  • Meningo-Oculo-Facial Angiomatosis
  • Neuroretinoangiomatosis
  • Parkes Weber Syndrome
  • Parkes-Weber Syndrome
  • Phakomatosis, Sturge-Weber
  • Sturge Disease
  • Sturge-Kalischer-Weber Syndrome
  • Sturge's Syndrome
  • Sturge Syndrome
  • Sturge-Weber-Dimitri Syndrome
  • Sturge-Weber-Krabbe Syndrome

Allowable Qualifier(s)

In other languages

  • Syndrome de Sturge-Weber

    French

  • Angiomatose congénitale de Sturge-Weber-Krabbe
  • Angiomatose encéphalo-trigéminée
  • Angiomatose encéphalotrigéminée
  • Maladie de Sturge-Weber-Krabbe
  • Neuro-angiomatose encéphalo-faciale
  • Neuroangiomatose encéphalofaciale
  • Phacomatose de Sturge-Weber-Krabbe
  • SWK (Syndrome de Sturge-Weber-Krabbe)
  • Syndrome de Sturge-Weber-Krabbe

URI

http://data.loterre.fr/ark:/67375/JVR-ZCL90G3X-N

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