{
    "disease_id": "DOID:0060671", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011305", 
            "name": "PDCD10 familial cerebral cavernous malformation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011305", 
            "name": "cerebral cavernous malformation type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011305", 
            "name": "cerebral cavernous malformations 3; CCM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011305", 
            "name": "familial cerebral cavernous malformation caused by mutation in PDCD10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011305", 
            "name": "cerebral cavernous malformations type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011305", 
            "name": "CCM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011305", 
            "name": "cerebral cavernous malformations 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060671", 
        "description": "A cerebral cavernous malformation that_has_material_basis in mutation in the PDCD10 gene on chromosome 3q26.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060671", 
        "name": "cerebral cavernous malformation 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060671#disease-associations", 
            "id": "0060671", 
            "database": "Alliance of Genome Resources"
        }
    ]
}