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Cardiovascular Diseases > Vascular Diseases > Angiomatosis > Sturge-Weber Syndrome
Nervous System Diseases > Neurocutaneous Syndromes > Sturge-Weber Syndrome
... > Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > 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
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > 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

Preferred term

Sturge-Weber Syndrome  

Type

  • Topical Descriptor

Broader concept

Entry terms

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

Scope note

  • 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.

History note

  • 91(75); was see under ANGIOMATOSIS 1975-90; DIMITRI DISEASE was see STURGE-WEBER SYNDROME 1989-93

In other languages

URI

http://www.yso.fi/onto/mesh/D013341

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