{
    "disease_id": "DOID:0080537", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014864", 
            "name": "SLC39A14 hypermanganesemia with dystonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014864", 
            "name": "hypermanganesemia with dystonia 2; HMNDYT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014864", 
            "name": "hypermanganesemia with dystonia type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014864", 
            "name": "hypermanganesemia with dystonia caused by mutation in SLC39A14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014864", 
            "name": "HMNDYT2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080537", 
        "description": "A hypermanganesemia with dystonia that is characterized predominantly by loss of motor milestones in the first years of life and has_material_basis_in homozygous mutation in the SLC39A14 gene on chromosome 8p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080537", 
        "name": "hypermanganesemia with dystonia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617013", 
            "id": "617013", 
            "database": "MIM"
        }
    ]
}