Preferred Name

Sturge-Weber Syndrome [Disease/Finding]

Synonyms

Parkes Weber Syndrome

ID

http://purl.bioontology.org/ontology/NDFRT/N0000002843

altLabel

Parkes Weber Syndrome

Meningo-Oculo-Facial Angiomatosis

Neuroretinoangiomatosis

Sturge Syndrome

Sturge-Weber-Krabbe Syndrome

Phakomatosis, Sturge-Weber

Sturge-Weber Syndrome

Sturge's Syndrome

Encephalofacial Hemangiomatosis Syndrome

Parkes-Weber Syndrome

Meningofacial Angiomatosis-Cerebral Calcification Syndrome

Sturge Disease

Angiomatosis Oculoorbital-Thalamic Syndrome

Sturge-Weber-Dimitri Syndrome

Sturge-Kalischer-Weber Syndrome

cui

C0038505

MESH 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.

MESH DUI

D013341

MeSH name

Sturge-Weber Syndrome

MESH UI

M0020641

NDFRT kind

DISEASE_KIND

notation

N0000002843

NUI

N0000002843

prefLabel

Sturge-Weber Syndrome [Disease/Finding]

SNOMED CID

19886006

234143003

tui

T019

subClassOf

http://purl.bioontology.org/ontology/NDFRT/N0000000414

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