{
    "disease_id": "DOID:0110144",
    "recommended_name": {
        "id": "DOID:0110144",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110144",
        "name": "Bartter disease type 3",
        "description": "A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36."
    },
    "synonyms": [
        {
            "id": "DOID:0110144",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110144",
            "name": "BARTS3",
            "description": ""
        },
        {
            "id": "DOID:0110144",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110144",
            "name": "Bartter syndrome type 3",
            "description": ""
        },
        {
            "id": "DOID:0110144",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110144",
            "name": "classic Bartter syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011822",
            "name": "Bartter disease type 3",
            "description": "Classic Bartter syndrome is a type of Bartter syndrome, characterized by a milder clinical picture than the antenatal/infantile subtype, and presenting with failure to thrive, hypokalemic alkalosis, increased levels of plasma renin and aldosterone, low blood pressure and vascular resistance to angiotensin II."
        },
        {
            "id": "MONDO:0011822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011822",
            "name": "BARTS3",
            "description": ""
        },
        {
            "id": "MONDO:0011822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011822",
            "name": "Bartter disease type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011822",
            "name": "Bartter syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011822",
            "name": "Bartter syndrome type III",
            "description": ""
        },
        {
            "id": "MONDO:0011822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011822",
            "name": "adult Bartter syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011822",
            "name": "Bartter syndrome classic",
            "description": ""
        },
        {
            "id": "MIM:607364",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607364",
            "name": "Bartter syndrome 3",
            "description": "Bartter syndrome 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110144"
    ],
    "unlinked_id_list": []
}