{
    "disease_id": "DOID:0110825",
    "recommended_name": {
        "id": "DOID:0110825",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110825",
        "name": "hereditary spastic paraplegia 9B",
        "description": "A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24."
    },
    "synonyms": [
        {
            "id": "DOID:0110825",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110825",
            "name": "autosomal recessive complex spastic paraplegia type 9B",
            "description": ""
        },
        {
            "id": "DOID:0110825",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110825",
            "name": "SPG9B",
            "description": ""
        },
        {
            "id": "DOID:0110825",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110825",
            "name": "autosomal recessive spastic paraplegia 9B",
            "description": ""
        },
        {
            "id": "MONDO:0014702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014702",
            "name": "autosomal recessive complex spastic paraplegia type 9B",
            "description": "Any autosomal recessive complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene."
        },
        {
            "id": "MONDO:0014702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014702",
            "name": "ALDH18A1 autosomal recessive complex spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0014702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014702",
            "name": "AR-SPG9B",
            "description": ""
        },
        {
            "id": "MONDO:0014702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014702",
            "name": "SPG9B",
            "description": ""
        },
        {
            "id": "MONDO:0014702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014702",
            "name": "autosomal recessive complex spastic paraplegia caused by mutation in ALDH18A1",
            "description": ""
        },
        {
            "id": "MONDO:0014702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014702",
            "name": "hereditary spastic paraplegia type 9B",
            "description": ""
        },
        {
            "id": "MONDO:0014702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014702",
            "name": "spastic paraplegia 9B, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:616586",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616586",
            "name": "Spastic paraplegia 9B, autosomal recessive",
            "description": "Spastic paraplegia 9B, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110825"
    ],
    "unlinked_id_list": []
}