{
    "disease_id": "DOID:2512", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007187", 
            "name": "multiple basal cell nevi, odontogenic keratocysts, and skeletal anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007187", 
            "name": "Gorlin-Goltz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007187", 
            "name": "basal cell nevus syndrome; BCNS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007187", 
            "name": "basal cell nevus syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007187", 
            "name": "nevoid basal cell cancer syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007187", 
            "name": "NBCCS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007187", 
            "name": "Gorlin syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007187", 
            "name": "multiple basal cell carcinomas"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007187", 
            "name": "BCNS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2512", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2512", 
            "name": "Gorlin syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2512", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2512", 
            "name": "NBCCS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2512", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2512", 
            "name": "basal cell nevus syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2512", 
        "description": "A syndrome characterized by multiple early-onset basal cell carcinoma, multiple jaw keratocysts and skeletal abnormalities that has_material_basis_in heterozygous mutation in either PTCH1, PTCH2, or SUFU on chromosome 9q22, 1p32, or 10q24-q25, respectively.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2512", 
        "name": "nevoid basal cell carcinoma syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2512#disease-associations", 
            "id": "2512", 
            "database": "Alliance of Genome Resources"
        }
    ]
}