{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013718", 
            "name": "nephronophthisis type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013718", 
            "name": "NPHP13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013718", 
            "name": "nephronophthisis 13; NPHP13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111121", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111121", 
            "name": "NPHP13"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111121", 
        "description": "A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the WDR19 gene on chromosome 4p14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111121", 
        "name": "nephronophthisis 13"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614377", 
            "id": "614377", 
            "database": "MIM"
        }
    ]
}