{
    "disease_id": "DOID:0110144", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011822", 
            "name": "Bartter syndrome, classic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011822", 
            "name": "Bartter syndrome classic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011822", 
            "name": "adult Bartter syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011822", 
            "name": "Bartter syndrome, type 3; BARTS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011822", 
            "name": "Bartter syndrome type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011822", 
            "name": "BARTS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011822", 
            "name": "Bartter syndrome, type 3, with hypocalciuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011822", 
            "name": "Bartter syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011822", 
            "name": "classic Bartter syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011822", 
            "name": "Bartter syndrome, type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110144", 
            "name": "BARTS3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110144", 
            "name": "Bartter syndrome type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110144", 
            "name": "classic Bartter syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110144", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110144", 
        "name": "Bartter disease type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110144#disease-associations", 
            "id": "0110144", 
            "database": "Alliance of Genome Resources"
        }
    ]
}