- Concept UI
- M0020641
- 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.
- Terms
-
Sturge-Weber Syndrome
Preferred Term
Term UI
T039175
Date01/01/1999
LexicalTag
EPO
ThesaurusID
-
Phakomatosis, Sturge-Weber
Term UI
T370611
Date11/03/1999
LexicalTag
EPO
ThesaurusID
NLM (2000)
-
Sturge Disease
Term UI
T370615
Date11/03/1999
LexicalTag
EPO
ThesaurusID
NLM (2000)
-
Sturge Syndrome
Term UI
T039172
Date05/23/1988
LexicalTag
EPO
ThesaurusID
UNK (19XX)
-
Sturge's Syndrome
Term UI
T039173
Date05/09/1988
LexicalTag
EPO
ThesaurusID
UNK (19XX)
-
Sturge-Kalischer-Weber Syndrome
Term UI
T039174
Date05/09/1988
LexicalTag
EPO
ThesaurusID
UNK (19XX)
-
Sturge-Weber-Dimitri Syndrome
Term UI
T039176
Date04/01/1993
LexicalTag
EPO
ThesaurusID
NLM (1994)
-
Sturge-Weber-Krabbe Syndrome
Term UI
T370616
Date11/03/1999
LexicalTag
EPO
ThesaurusID
NLM (2000)
-
Angiomatosis Oculoorbital-Thalamic Syndrome
Term UI
T370612
Date11/03/1999
LexicalTag
NON
ThesaurusID
NLM (2000)
-
Encephalofacial Hemangiomatosis Syndrome
Term UI
T372483
Date11/03/1999
LexicalTag
NON
ThesaurusID
NLM (2000)
-
Meningo-Oculo-Facial Angiomatosis
Term UI
T370613
Date11/03/1999
LexicalTag
NON
ThesaurusID
NLM (2000)
-
Meningofacial Angiomatosis-Cerebral Calcification Syndrome
Term UI
T370614
Date11/03/1999
LexicalTag
NON
ThesaurusID
NLM (2000)
-
Neuroretinoangiomatosis
Term UI
T370610
Date11/03/1999
LexicalTag
NON
ThesaurusID
NLM (2000)