{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000909", 
            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000909", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000909", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000909", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000909", 
            "name": "Bartter syndrome, infantile, with sensorineural deafness"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000909", 
            "name": "BARTS4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000909", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000909", 
            "name": "Bartter syndrome, type 4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000909", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000909", 
            "name": "Bartter syndrome, type 4B, neonatal, with sensorineural deafness; BARTS4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0000909", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0000909", 
            "name": "neonatal Bartter syndrome type 4B with sensorineural deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110146", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110146", 
            "name": "neonatal Bartter syndrome type 4B with sensorineural deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110146", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110146", 
            "name": "BARTS4B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110146", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110146", 
            "name": "Bartter syndrome, type 4b, digenic"
        }, 
        {
            "url": "https://www.omim.org/entry/613090", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613090", 
            "name": "Bartter syndrome 4B, neonatal, with sensorineural deafness"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110146", 
        "description": "A Bartter disease that has_material_basis_in simultaneous mutation in both the CLCNKA and CLCNKB genes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110146", 
        "name": "Bartter disease type 4b"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613090", 
            "id": "613090", 
            "database": "MIM"
        }
    ]
}