{
    "disease_id": "DOID:0060160",
    "recommended_name": {
        "id": "DOID:0060160",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060160",
        "name": "childhood spinal muscular atrophy",
        "description": "A spinal muscular atrophy that is associated with the survival of motor neuron protein in childhood and that has_material_basis_in variation in the SMN gene."
    },
    "synonyms": [
        {
            "id": "DOID:0060160",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060160",
            "name": "spinal muscular atrophies of childhood",
            "description": ""
        },
        {
            "id": "DOID:0060160",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060160",
            "name": "survival motor neuron spinal muscular atrophy",
            "description": ""
        }
    ],
    "children": [
        {
            "id": "DOID:0050530",
            "label": "intermediate spinal muscular atrophy",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:12376",
            "label": "juvenile spinal muscular atrophy",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:13137",
            "label": "Werdnig-Hoffmann disease",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0050530",
        "DOID:0060160",
        "DOID:12376",
        "DOID:13137"
    ],
    "unlinked_id_list": []
}