MeSH Browser

MeSH Heading: Sturge-Weber Syndrome
Tree Number(s): C04.557.645.375.850; C10.562.800; C14.907.077.850
Unique ID: D013341
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D013341
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.
Entry Term(s): Angiomatosis Oculoorbital-Thalamic Syndrome; Encephalofacial Hemangiomatosis Syndrome; Meningo-Oculo-Facial Angiomatosis; Meningofacial Angiomatosis-Cerebral Calcification Syndrome; Neuroretinoangiomatosis; Parkes Weber Syndrome; Parkes-Weber Syndrome; Phakomatosis, Sturge-Weber; Sturge Disease; Sturge Syndrome; Sturge's Syndrome; Sturge-Kalischer-Weber Syndrome; Sturge-Weber-Dimitri Syndrome; Sturge-Weber-Krabbe Syndrome
Public MeSH Note: 91; was see under ANGIOMATOSIS 1975-90; DIMITRI DISEASE was see STURGE-WEBER SYNDROME 1989-93
Online Note: search ANGIOMATOSIS 1966-74; use STURGE-WEBER SYNDROME to search DIMITRI DISEASE 1989-93
History Note: 91(75); was see under ANGIOMATOSIS 1975-90; DIMITRI DISEASE was see STURGE-WEBER SYNDROME 1989-93
Date Established: 1991/01/01
Date of Entry: 1999/01/01
Revision Date: 2023/04/26

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Neoplasms [C04]
- Neoplasms by Histologic Type [C04.557]
  - Neoplasms, Vascular Tissue [C04.557.645]
    - Hemangioma [C04.557.645.375]

Nervous System Diseases [C10]
- Neurocutaneous Syndromes [C10.562]

Cardiovascular Diseases [C14]
- Vascular Diseases [C14.907]
  - Angiomatosis [C14.907.077]

Sturge-Weber Syndrome Preferred

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)

Parkes Weber Syndrome Narrower

Sturge-Weber Syndrome MeSH Descriptor Data 2025