{
    "disease_id": "DOID:0080536", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013208", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013208", 
            "name": "cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013208", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013208", 
            "name": "hypermanganesemia with dystonia, polycythemia, and cirrhosis; HMDPC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013208", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013208", 
            "name": "HMDPC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013208", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013208", 
            "name": "hypermanganesemia with dystonia polycythemia and cirrhosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013208", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013208", 
            "name": "HMNDYT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013208", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013208", 
            "name": "hypermanganesemia with dystonia 1; HMNDYT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013208", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013208", 
            "name": "hypermanganesemia with dystonia, polycythemia, and cirrhosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080536", 
        "description": "A hypermanganesemia with dystonia that is characterized by increased serum manganese, motor neurodegeneration with extrapyramidal features, polycythemia, and hepatic dysfunction and has_material_basis_in homozygous mutation in the SLC30A10 gene on chromosome 1q41.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080536", 
        "name": "hypermanganesemia with dystonia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080536#disease-associations", 
            "id": "0080536", 
            "database": "Alliance of Genome Resources"
        }
    ]
}