{
    "disease_id": "DOID:0110142",
    "recommended_name": {
        "id": "DOID:0110142",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110142",
        "name": "Bartter disease type 1",
        "description": "A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the sodium-potassium-chloride cotransporter-2 gene (SLC12A1) on chromosome 15q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110142",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110142",
            "name": "hypokalemic alkalosis with hypercalciuria 1 antenatal",
            "description": ""
        },
        {
            "id": "DOID:0110142",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110142",
            "name": "BARTS1",
            "description": ""
        },
        {
            "id": "DOID:0110142",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110142",
            "name": "Bartter syndrome type 1",
            "description": ""
        },
        {
            "id": "DOID:0110142",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110142",
            "name": "Bartter syndrome type 1 antenatal",
            "description": ""
        },
        {
            "id": "DOID:0110142",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110142",
            "name": "hyperprostaglandin E syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "Bartter disease type 1",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "Bartter syndrome, furosemide type",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "Bartter syndrome, furosemide-amiloride type",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "hyperprostaglandin E syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "BARTS1",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "Bartter disease type 1",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "Bartter syndrome caused by mutation in SLC12A1",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "Bartter syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "Bartter syndrome, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "SLC12A1 Bartter syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "hyperprostaglandin E syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "Bartter syndrome antenatal type 1",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "antenatal Bartter syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0100344",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100344",
            "name": "hypokalemic alkalosis with hypercalciuria antenatal 1",
            "description": ""
        },
        {
            "id": "MIM:601678",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601678",
            "name": "Bartter syndrome 1, antenatal",
            "description": "Bartter syndrome 1, antenatal"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110142"
    ],
    "unlinked_id_list": []
}