{
    "disease_id": "DOID:0080759",
    "recommended_name": {
        "id": "DOID:0080759",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080759",
        "name": "Fanconi renotubular syndrome 3",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0014275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014275",
            "name": "Fanconi renotubular syndrome 3",
            "description": "Any Fanconi syndrome in which the cause of the disease is a mutation in the EHHADH gene."
        },
        {
            "id": "MONDO:0014275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014275",
            "name": "EHHADH Fanconi syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014275",
            "name": "Fanconi renotubular syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0014275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014275",
            "name": "Fanconi renotubular syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0014275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014275",
            "name": "Fanconi syndrome caused by mutation in EHHADH",
            "description": ""
        },
        {
            "id": "MONDO:0014275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014275",
            "name": "FRTS3",
            "description": ""
        },
        {
            "id": "MIM:615605",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615605",
            "name": "Fanconi renotubular syndrome 3",
            "description": "Fanconi renotubular syndrome 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080759"
    ],
    "unlinked_id_list": []
}