{
    "disease_id": "DOID:0110781",
    "recommended_name": {
        "id": "DOID:0110781",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110781",
        "name": "hereditary spastic paraplegia 30",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF1A gene on chromosome 2q37."
    },
    "synonyms": [
        {
            "id": "DOID:0110781",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110781",
            "name": "SPG30",
            "description": ""
        },
        {
            "id": "DOID:0110781",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110781",
            "name": "autosomal spastic paraplegia type 30",
            "description": ""
        }
    ],
    "children": [
        {
            "id": "DOID:0070646",
            "label": "hereditary spastic paraplegia 30B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070647",
            "label": "hereditary spastic paraplegia 30A",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0070647",
        "DOID:0110781",
        "DOID:0070646"
    ],
    "unlinked_id_list": []
}