{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014771", 
            "name": "Joubert syndrome 26; JBTS26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014771", 
            "name": "KIAA0556 Joubert syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014771", 
            "name": "Joubert syndrome caused by mutation in KIAA0556"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014771", 
            "name": "Joubert syndrome type 26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014771", 
            "name": "JBTS26"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110995", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110995", 
            "name": "JBTS26"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110995", 
        "description": "A Joubert syndrome characterized by global developmental delay and cerebellar hypoplasia that has_material_basis_in homozygous mutation in the KIAA0556 gene on chromosome 16p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110995", 
        "name": "Joubert syndrome 26"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616784", 
            "id": "616784", 
            "database": "MIM"
        }
    ]
}