{
    "disease_id": "DOID:0080550", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013380", 
            "name": "LEOPARD syndrome 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013380", 
            "name": "BRAF Noonan syndrome with multiple lentigines"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013380", 
            "name": "LPRD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013380", 
            "name": "Leopard syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013380", 
            "name": "LEOPARD syndrome 3; LPRD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013380", 
            "name": "Noonan syndrome with multiple lentigines caused by mutation in BRAF"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080550", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080550", 
            "name": "LEOPARD syndrome 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080550", 
        "description": "A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the BRAF gene on chromosome 7q34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080550", 
        "name": "Noonan syndrome with multiple lentigines 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080550#disease-associations", 
            "id": "0080550", 
            "database": "Alliance of Genome Resources"
        }
    ]
}