{
    "disease_id": "DOID:0080758", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013247", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013247", 
            "name": "Fanconi renotubular syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013247", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013247", 
            "name": "FRTS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013247", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013247", 
            "name": "Fanconi syndrome caused by mutation in SLC34A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013247", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013247", 
            "name": "SLC34A1 Fanconi syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013247", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013247", 
            "name": "Fanconi renotubular syndrome 2; FRTS2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080758", 
        "description": "A Fanconi syndrome that has_material_basis_in homozygous mutation in the SLC34A1 gene on chromosome 5q35.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080758", 
        "name": "Fanconi renotubular syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613388", 
            "id": "613388", 
            "database": "MIM"
        }
    ]
}