{
    "disease_id": "DOID:0110147",
    "recommended_name": {
        "id": "DOID:0110147",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110147",
        "name": "Bartter disease type 5",
        "description": "A Bartter disease that has_material_basis_in mutation in the MAGED2 gene on chromosome Xp11."
    },
    "synonyms": [
        {
            "id": "DOID:0110147",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110147",
            "name": "BARTS5",
            "description": ""
        },
        {
            "id": "DOID:0110147",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110147",
            "name": "Bartter syndrome, type 5, antenatal, transient",
            "description": ""
        },
        {
            "id": "MONDO:0010503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010503",
            "name": "Bartter disease type 5",
            "description": "Any Bartter syndrome in which the cause of the disease is a mutation in the MAGED2 gene."
        },
        {
            "id": "MONDO:0010503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010503",
            "name": "Bartter syndrome, type 5, antenatal, transient; BARTS5",
            "description": ""
        },
        {
            "id": "MONDO:0010503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010503",
            "name": "MAGED2 Bartter syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010503",
            "name": "BARTS5",
            "description": ""
        },
        {
            "id": "MONDO:0010503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010503",
            "name": "Bartter syndrome caused by mutation in MAGED2",
            "description": ""
        },
        {
            "id": "MONDO:0010503",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010503",
            "name": "Bartter syndrome, type 5, antenatal, transient",
            "description": ""
        },
        {
            "id": "MIM:300971",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300971",
            "name": "Bartter syndrome 5, antenatal, transient",
            "description": "Bartter syndrome 5, antenatal, transient"
        }
    ]
}