{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "Sturge-Weber-Dimitri syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
            "name": "Encephalotrigeminal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
            "name": "SWS type III - isolated leptomeningeal angiomas"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
            "name": "Sturge Weber syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
            "name": "STURGE-WEBER syndrome; SWS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
            "name": "SWS type II - Facial angioma alone, no CNS involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
            "name": "Encephalotrigeminal angiomatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
            "name": "SWS type I - Facial and leptomeningeal angiomas"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
            "name": "Sturge-Weber-Krabbe syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
            "name": "Sturge-Weber-Krabbe angiomatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008501", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008501", 
            "name": "leptomeningeal angiomatosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111563", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111563", 
            "name": "SWS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111563", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111563", 
            "name": "Sturge-Weber-Dimitri syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111563", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111563", 
            "name": "Sturge-Weber-Krabbe angiomatosis"
        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111563", 
            "name": "Sturge-Weber-Krabbe syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111563", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111563", 
            "name": "encephalofacial angiomatosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111563", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111563", 
            "name": "encephalotrigeminal angiomatosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111563", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111563", 
            "name": "fourth phacomatosis"
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        {
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            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "leptomeningeal angiomatosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111563", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111563", 
            "name": "meningeal capillary angiomatosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111563", 
        "description": "A vascular disease characterized by intracranial vascular anomaly, leptomeningeal angiomatosis, facial cutaneous vascular malformations, and glaucoma that has_material_basis_in somatic mutation in GNAQ on chromosome 9q21.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111563", 
        "name": "Sturge-Weber syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/185300", 
            "id": "185300", 
            "database": "MIM"
        }
    ]
}