{
    "disease_id": "DOID:0080537",
    "recommended_name": {
        "id": "DOID:0080537",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080537",
        "name": "hypermanganesemia with dystonia 2",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0014864",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014864",
            "name": "hypermanganesemia with dystonia 2",
            "description": "Any hypermanganesemia with dystonia in which the cause of the disease is a mutation in the SLC39A14 gene."
        },
        {
            "id": "MONDO:0014864",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014864",
            "name": "HMNDYT2",
            "description": ""
        },
        {
            "id": "MONDO:0014864",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014864",
            "name": "SLC39A14 hypermanganesemia with dystonia",
            "description": ""
        },
        {
            "id": "MONDO:0014864",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014864",
            "name": "hypermanganesemia with dystonia 2",
            "description": ""
        },
        {
            "id": "MONDO:0014864",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014864",
            "name": "hypermanganesemia with dystonia 2; HMNDYT2",
            "description": ""
        },
        {
            "id": "MONDO:0014864",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014864",
            "name": "hypermanganesemia with dystonia caused by mutation in SLC39A14",
            "description": ""
        },
        {
            "id": "MONDO:0014864",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014864",
            "name": "hypermanganesemia with dystonia type 2",
            "description": ""
        },
        {
            "id": "MIM:617013",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617013",
            "name": "Hypermanganesemia with dystonia 2",
            "description": "Hypermanganesemia with dystonia 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080537"
    ],
    "unlinked_id_list": []
}