{
    "disease_id": "DOID:0110145",
    "recommended_name": {
        "id": "DOID:0110145",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110145",
        "name": "Bartter disease type 4a",
        "description": "A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the BSND gene on chromosome 1p32."
    },
    "synonyms": [
        {
            "id": "DOID:0110145",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110145",
            "name": "BARTS4A",
            "description": ""
        },
        {
            "id": "DOID:0110145",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110145",
            "name": "BSND",
            "description": ""
        },
        {
            "id": "DOID:0110145",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110145",
            "name": "Bartter syndrome type 4a",
            "description": ""
        },
        {
            "id": "DOID:0110145",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110145",
            "name": "neonatal Bartter syndrome with sensorineural deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "Bartter disease type 4A",
            "description": "Any Bartter syndrome in which the cause of the disease is a mutation in the BSND gene."
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "BARTS4A",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "BSND",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "BSND Bartter syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "Bartter disease type 4a",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "Bartter syndrome caused by mutation in BSND",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "Bartter syndrome type 4a",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "neonatal Bartter syndrome with sensorineural deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "Bartter syndrome, infantile, with sensorineural deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "Bartter syndrome, neonatal, with sensorineural deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "Bartter syndrome, type 4A",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "Bartter syndrome, type 4A, neonatal, with sensorineural deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011242",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011242",
            "name": "sensorineural deafness with mild renal dysfunction",
            "description": ""
        },
        {
            "id": "MIM:602522",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/602522",
            "name": "Bartter syndrome 4A, neonatal, with sensorineural deafness",
            "description": "Bartter syndrome 4A, neonatal, with sensorineural deafness"
        }
    ]
}