{
    "disease_id": "DOID:0060911", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013898", 
            "name": "interstitial nephritis caused by mutation in FAN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013898", 
            "name": "kin"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013898", 
            "name": "FAN1 interstitial nephritis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013898", 
            "name": "KMIN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013898", 
            "name": "systemic karyomegaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013898", 
            "name": "interstitial nephritis, karyomegalic; KMIN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013898", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013898", 
            "name": "interstitial nephritis, karyomegalic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060911", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060911", 
            "name": "KIN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060911", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060911", 
            "name": "KMIN"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060911", 
        "description": "An interstitial nephritis characterized by nephritis, interstitial fibrosis, and enlarged and atypical tubular epithelial cell nuclei that has_material_basis_in homozygous or compound heterozygous mutation in the FAN1 gene on chromosome 15q13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060911", 
        "name": "karyomegalic interstitial nephritis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060911#disease-associations", 
            "id": "0060911", 
            "database": "Alliance of Genome Resources"
        }
    ]
}