{
    "disease_id": "DOID:1062", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024525", 
            "name": "FRTS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024525", 
            "name": "Fanconi renotubular syndrome 1; FRTS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024525", 
            "name": "Fanconi renotubular syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024525", 
            "name": "renal Fanconi syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024525", 
            "name": "Luder-Sheldon syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024525", 
            "name": "adult Fanconi syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024525", 
            "name": "Fanconi syndrome without cystinosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1062", 
            "name": "Congenital Fanconi syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1062", 
            "name": "De Toni-Fanconi syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1062", 
            "name": "Fanconi-de Toni syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1062", 
            "name": "Fanconi-de-Toni syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1062", 
            "name": "Infantile nephropathic cystinosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1062", 
            "name": "Lignac-Fanconi syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1062", 
            "name": "adult Fanconi Anemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1062", 
            "name": "adult Fanconi syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1062", 
            "name": "deToni Fanconi syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1062", 
        "description": "A renal tubular transport disease of the proximal renal tubes characterized by glucosuria, phosphaturia, generalized aminoaciduria and HCO3 wasting.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1062", 
        "name": "Fanconi syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/1062#disease-associations", 
            "id": "1062", 
            "database": "Alliance of Genome Resources"
        }
    ]
}