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 |