{
    "disease_id": "DOID:0070490",
    "recommended_name": {
        "id": "DOID:0070490",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070490",
        "name": "infantile parkinsonism-dystonia 2",
        "description": "A movement disease characterized by parkinsonism, dystonia, poor fine motor skills, and autonomic dysfunction including abnormal sweating, cold extremities, and poor sleep that has_material_basis_in homozygous mutation in the SLC18A2 gene on chromosome 10q25.3."
    },
    "synonyms": [
        {
            "id": "DOID:0070490",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070490",
            "name": "PKDYS2",
            "description": ""
        },
        {
            "id": "DOID:0070490",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070490",
            "name": "Brain dopamine-serotonin vesicular transport disease",
            "description": ""
        },
        {
            "id": "MONDO:0018130",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018130",
            "name": "brain dopamine-serotonin vesicular transport disease",
            "description": "An infantile-onset neurometabolic disease characterized by dystonia, parkinsonism, nonambulation, autonomic dysfunction, developmental delay and mood disturbances."
        },
        {
            "id": "MONDO:0018130",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018130",
            "name": "PKDYS2",
            "description": ""
        },
        {
            "id": "MONDO:0018130",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018130",
            "name": "parkinsonism-dystonia, infantile, 2",
            "description": ""
        },
        {
            "id": "MIM:618049",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618049",
            "name": "Parkinsonism-dystonia 2, infantile-onset",
            "description": "Parkinsonism-dystonia 2, infantile-onset"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070490"
    ],
    "unlinked_id_list": []
}