{
    "disease_id": "DOID:0111119", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013442", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013442", 
            "name": "nephronophthisis (disease) caused by mutation in TTC21B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013442", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013442", 
            "name": "TTC21B nephronophthisis (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013442", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013442", 
            "name": "nephronophthisis type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013442", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013442", 
            "name": "NPHP12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013442", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013442", 
            "name": "nephronophthisis 12; NPHP12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013442", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013442", 
            "name": "Joubert syndrome 11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111119", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111119", 
            "name": "NPHP12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111119", 
        "description": "A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the TTC21B gene on chromosome 2q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111119", 
        "name": "nephronophthisis 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613820", 
            "id": "613820", 
            "database": "MIM"
        }
    ]
}