{
    "disease_id": "DOID:0110787",
    "recommended_name": {
        "id": "DOID:0110787",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110787",
        "name": "hereditary spastic paraplegia 36",
        "description": "A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 12q23-q24."
    },
    "synonyms": [
        {
            "id": "DOID:0110787",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110787",
            "name": "SPG36",
            "description": ""
        },
        {
            "id": "DOID:0110787",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110787",
            "name": "autosomal dominant spastic paraplegia 36",
            "description": ""
        },
        {
            "id": "DOID:0110787",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110787",
            "name": "autosomal dominant spastic paraplegia type 36",
            "description": ""
        },
        {
            "id": "MONDO:0013132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013132",
            "name": "hereditary spastic paraplegia 36",
            "description": "Autosomal dominant spastic paraplegia type 36 (SPG36) is a complex form of hereditary spastic paraplegia, characterized by an onset in childhood or adulthood of progressive spastic paraplegia (with spastic gait, spasticity, lower limb weakness, pes cavus and urinary urgency) associated with the additional manifestation of peripheral sensorimotor neuropathy."
        },
        {
            "id": "MONDO:0013132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013132",
            "name": "hereditary spastic paraplegia type 36",
            "description": ""
        },
        {
            "id": "MONDO:0013132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013132",
            "name": "SPG36",
            "description": ""
        },
        {
            "id": "MONDO:0013132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013132",
            "name": "spastic paraplegia 36, autosomal dominant; SPG36",
            "description": ""
        },
        {
            "id": "MONDO:0013132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013132",
            "name": "autosomal dominant spastic paraplegia 36",
            "description": ""
        },
        {
            "id": "MONDO:0013132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013132",
            "name": "spastic paraplegia 36, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0013132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013132",
            "name": "autosomal dominant spastic paraplegia type 36",
            "description": ""
        }
    ]
}