{
    "disease_id": "DOID:0070718",
    "recommended_name": {
        "id": "DOID:0070718",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070718",
        "name": "neurodevelopmental disorder with behavioral abnormalities and childhood-onset spastic paraplegia",
        "description": "A hereditary spastic paraplegia characterized by mild global developmental delay apparent from infancy, with mildly delayed walking and speech acquisition, mildly impaired intellectual development, behavioral abnormalities, and age-dependent, slowly progressive spastic paraplegia late in the first decade, resulting in gait abnormalities but not loss of ambulation, that has_material_basis_in homozygous mutation in the TBCB gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070718",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070718",
            "name": "NEDBSPG",
            "description": ""
        },
        {
            "id": "MONDO:0980706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980706",
            "name": "neurodevelopmental disorder with behavioral abnormalities and childhood-onset spastic paraplegia",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070718"
    ],
    "unlinked_id_list": []
}