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