{
    "disease_id": "DOID:0111004", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012849", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012849", 
            "name": "Joubert syndrome 9; JBTS9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012849", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012849", 
            "name": "Joubert syndrome 9/15, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012849", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012849", 
            "name": "JBTS9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012849", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012849", 
            "name": "Joubert syndrome caused by mutation in CC2D2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012849", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012849", 
            "name": "Joubert syndrome type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012849", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012849", 
            "name": "CC2D2A Joubert syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111004", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111004", 
            "name": "JBTS9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111004", 
        "description": "A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CC2D2A gene on chromosome 4p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111004", 
        "name": "Joubert syndrome 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111004#disease-associations", 
            "id": "0111004", 
            "database": "Alliance of Genome Resources"
        }
    ]
}