Sturge–Weber syndrome
neurological and skin disorder associated with port-wine stains of the face, glaucoma, seizures, intellectual disability, and cerebral malformations
Sturge–Weber syndrome
Summary
Sturge–Weber syndrome is a rare disease[1] . It has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[2]
Key Facts
Sturge–Weber syndrome's instance of is recorded as rare disease[3] .
Sturge–Weber syndrome's instance of is recorded as head and neck disease[4] .
Sturge–Weber syndrome's instance of is recorded as developmental defect during embryogenesis[5] .
Sturge–Weber syndrome's instance of is recorded as designated intractable/rare disease[6] .
Sturge–Weber syndrome's instance of is recorded as class of disease[7] .
William Allen Sturge is named after Sturge–Weber syndrome[8] .
Frederick Parkes Weber is named after Sturge–Weber syndrome[9] .
Sturge–Weber syndrome is a type of phakomatosis[10] .
Sturge–Weber syndrome is a type of overgrowth syndrome[11] .
Sturge–Weber syndrome is a type of cerebral diseases of vascular origin with epilepsy[12] .
Sturge–Weber syndrome is a type of neurocutaneous syndrome with epilepsy[13] .
Sturge–Weber syndrome is a type of syndrome or malformation associated with head and neck malformations[14] .
Sturge–Weber syndrome is a type of skull cancer[15] .
Sturge–Weber syndrome is a type of brain cancer[16] .
Sturge–Weber syndrome is a type of rare capillary malformation with associated anomalies[17] .
Sturge–Weber syndrome is a type of palpebral tumor with a vascular malformation[18] .
Sturge–Weber syndrome is a type of rare genetic vascular tumor[19] .
Sturge–Weber syndrome is a type of conjunctival cancer[20] .
Sturge–Weber syndrome is a type of conjunctival hemangioma or hemolymphangioma[21] .
Sturge–Weber syndrome is a type of syndromic glaucoma[22] .
Sturge–Weber syndrome is a type of central nervous system vascular malformation[23] .
Sturge–Weber syndrome is a type of syndromic developmental defect of the eye[24] .
Sturge–Weber syndrome is a type of vascular disease[25] .
Sturge–Weber syndrome is a type of disease[26] .
Sturge–Weber syndrome's Commons category is recorded as Sturge–Weber syndrome[27] .
Why It Matters
Sturge–Weber syndrome has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[2] It is known by 52 alternative names across languages and contexts.[28]
⭐ Popularity Graph
2/100
established
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Quick Facts
Instance of
rare disease , designated intractable/rare disease, class of disease
Subclass of
phakomatosis , overgrowth syndrome , cerebral diseases of vascular origin with epilepsy, neurocutaneous syndrome with epilepsy, syndrome or malformation associated with head and neck malformations, skull cancer, brain cancer , rare capillary malformation with associated anomalies, palpebral tumor with a vascular malformation, rare genetic vascular tumor, conjunctival cancer , conjunctival hemangioma or hemolymphangioma, syndromic glaucoma, central nervous system vascular malformation, syndromic developmental defect of the eye, vascular disease , developmental defect during embryogenesis, head and neck disease
Properties
Icd-9-cm
759.6
Nci thesaurus id
C3391
External References (27)
Babelnet id
01888122n
Disease ontology id
DOID:0111563
Diseasesdb
12572
Emedicine id
1177523
Encyclopædia britannica online id
science/Sturge-Weber-syndrome
Freebase id
/m/07lxpk
Gard rare disease id
7706
Icd-10 id
Q85.8
Icd-10-cm
Q85.8
Icd-11 id (foundation)
1173035836
Icd-9 id
759.6
Jstor topic id (archived)
sturge-weber-syndrome
Kegg id
H01809
Medical dictionary for regulatory activities id
10048734
Medlineplus id
001426
Mesh descriptor id
D013341
Mesh tree code
C04.557.645.375.850, C10.562.800, C14.907.077.850
Microsoft academic id (discontinued)
2779301331
Mondo id
MONDO_0008501
Omim id
185300
Openalex id
C2779301331
Orphanet id
3205
Patientslikeme condition id
sturge-weber
Umls cui
C0038505
Uniprot disease id
DI-03787
Wikikids id
Syndroom_van_Sturge-Weber
Wikiprojectmed id
Sturge–Weber syndrome
🌐 Available in 15 languages
🏷️ Also known as
en SWS type III - Isolated leptomeningeal angiomas
en Encephalofacial angiomatosis
en encephalotrigeminal angiomatosis
en Encephalotrigeminal Syndrome
en Fourth phacomatosis
en Leptomeningeal angiomatosis
en Meningeal capillary angiomatosis
en Sturge-Weber-Dimitri syndrome
en Sturge-Weber Disease
en Sturge-Weber-Krabbe angiomatosis
en Sturge-Weber-Krabbe disease
en SWS type I - Facial and leptomeningeal angiomas
en SWS type II - Facial angioma alone, no CNS involvement
en Sturge-Weber-Krabbe syndrome
en Sturge Weber syndrome
en Sturge-Weber syndrome
en Sturge-Weber Syndrome
en STURGE-WEBER SYNDROME; SWS
en SWS
de Angiomatosis encephalofacialis
🔗 Connections
Subclass of
3
Named after
2
Genetic association
1
Health specialty
1
Instance of
1
← Genetic association
1