{
    "disease_id": "DOID:0110772",
    "recommended_name": {
        "id": "DOID:0110772",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110772",
        "name": "hereditary spastic paraplegia 19",
        "description": "A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 9q."
    },
    "synonyms": [
        {
            "id": "DOID:0110772",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110772",
            "name": "SPG19",
            "description": ""
        },
        {
            "id": "DOID:0110772",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110772",
            "name": "autosomal dominant spastic paraplegia 19",
            "description": ""
        },
        {
            "id": "DOID:0110772",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110772",
            "name": "autosomal dominant spastic paraplegia type 19",
            "description": ""
        },
        {
            "id": "MONDO:0011785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011785",
            "name": "hereditary spastic paraplegia 19",
            "description": "Autosomal dominant spastic paraplegia type 19 is a pure form of hereditary spastic paraplegia characterized by a slowly progressive and relatively benign spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction (urinary urgency and/or incontinence), and mild sensory and motor peripheral neuropathy."
        },
        {
            "id": "MONDO:0011785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011785",
            "name": "spastic paraplegia 19",
            "description": ""
        },
        {
            "id": "MONDO:0011785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011785",
            "name": "SPG19",
            "description": ""
        },
        {
            "id": "MONDO:0011785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011785",
            "name": "hereditary spastic paraplegia type 19",
            "description": ""
        },
        {
            "id": "MONDO:0011785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011785",
            "name": "spastic paraplegia 19, autosomal dominant; SPG19",
            "description": ""
        },
        {
            "id": "MONDO:0011785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011785",
            "name": "autosomal dominant spastic paraplegia 19",
            "description": ""
        },
        {
            "id": "MONDO:0011785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011785",
            "name": "autosomal dominant spastic paraplegia type 19",
            "description": ""
        },
        {
            "id": "MONDO:0011785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011785",
            "name": "spastic paraplegia 19, autosomal dominant",
            "description": ""
        }
    ]
}