{
    "disease_id": "DOID:0110984", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013763", 
            "name": "Joubert syndrome 12/15, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013763", 
            "name": "Joubert syndrome caused by mutation in CEP41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013763", 
            "name": "Joubert syndrome 9/15, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013763", 
            "name": "CEP41 Joubert syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013763", 
            "name": "Joubert syndrome type 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013763", 
            "name": "Joubert syndrome 15; JBTS15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013763", 
            "name": "JBTS15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110984", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110984", 
            "name": "JBTS15"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110984", 
        "description": "A Joubert syndrome characterized by ataxia, hypotonia, delayed psychomotor development, and variable mental retardation that has_material_basis_in homozygous mutation in the CEP41 gene on chromosome 7q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110984", 
        "name": "Joubert syndrome 15"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110984#disease-associations", 
            "id": "0110984", 
            "database": "Alliance of Genome Resources"
        }
    ]
}