{
    "disease_id": "DOID:0070647",
    "recommended_name": {
        "id": "DOID:0070647",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070647",
        "name": "hereditary spastic paraplegia 30A",
        "description": "A hereditary spastic paraplegia 30 that has_material_basis_in heterozygous mutation in the KIF1A gene on chromosome 2q37."
    },
    "synonyms": [
        {
            "id": "DOID:0070647",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070647",
            "name": "autosomal dominant spastic paraplegia 30",
            "description": ""
        },
        {
            "id": "DOID:0070647",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070647",
            "name": "spastic paraplegia 30A",
            "description": ""
        },
        {
            "id": "MONDO:0700307",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0700307",
            "name": "spastic paraplegia 30A, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:610357",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610357",
            "name": "Spastic paraplegia 30A, autosomal dominant",
            "description": "Spastic paraplegia 30A, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070647"
    ],
    "unlinked_id_list": []
}