{
    "disease_id": "DOID:0110823",
    "recommended_name": {
        "id": "DOID:0110823",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110823",
        "name": "hereditary spastic paraplegia 8",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the KIAA0196 gene on chromosome 8q24."
    },
    "synonyms": [
        {
            "id": "DOID:0110823",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110823",
            "name": "SPG8",
            "description": ""
        },
        {
            "id": "DOID:0110823",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110823",
            "name": "autosomal dominant spastic paraplegia 8",
            "description": ""
        },
        {
            "id": "DOID:0110823",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110823",
            "name": "autosomal dominant spastic paraplegia type 8",
            "description": ""
        },
        {
            "id": "MONDO:0011339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011339",
            "name": "hereditary spastic paraplegia 8",
            "description": "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the WASHC5 gene."
        },
        {
            "id": "MONDO:0011339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011339",
            "name": "SPG8",
            "description": ""
        },
        {
            "id": "MONDO:0011339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011339",
            "name": "WASHC5 hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0011339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011339",
            "name": "autosomal dominant spastic paraplegia type 8",
            "description": ""
        },
        {
            "id": "MONDO:0011339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011339",
            "name": "hereditary spastic paraplegia caused by mutation in WASHC5",
            "description": ""
        },
        {
            "id": "MONDO:0011339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011339",
            "name": "hereditary spastic paraplegia type 8",
            "description": ""
        },
        {
            "id": "MONDO:0011339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011339",
            "name": "spastic paraplegia 8",
            "description": ""
        },
        {
            "id": "MONDO:0011339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011339",
            "name": "spastic paraplegia 8, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:603563",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/603563",
            "name": "Spastic paraplegia 8, autosomal dominant",
            "description": "Spastic paraplegia 8, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110823"
    ],
    "unlinked_id_list": []
}