{
    "disease_id": "DOID:0080759", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014275", 
            "name": "Fanconi renotubular syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014275", 
            "name": "FRTS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014275", 
            "name": "EHHADH Fanconi syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014275", 
            "name": "Fanconi renotubular syndrome 3; FRTS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014275", 
            "name": "Fanconi syndrome caused by mutation in EHHADH"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080759", 
        "description": "A Fanconi syndrome that is characterized by characterized by rickets, impaired growth, glucosuria, generalized aminoaciduria, phosphaturia, metabolic acidosis, and low molecular weight proteinuria and that has_material_basis_in heterozygous mutation in the EHHADH gene on chromosome 3q27.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080759", 
        "name": "Fanconi renotubular syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615605", 
            "id": "615605", 
            "database": "MIM"
        }
    ]
}