{
    "disease_id": "DOID:0110771",
    "recommended_name": {
        "id": "DOID:0110771",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110771",
        "name": "hereditary spastic paraplegia 18",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11."
    },
    "synonyms": [
        {
            "id": "DOID:0110771",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110771",
            "name": "intellectual disability, motor dysfunction and joint contractures",
            "description": ""
        },
        {
            "id": "DOID:0110771",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110771",
            "name": "IDMDC",
            "description": ""
        },
        {
            "id": "DOID:0110771",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110771",
            "name": "SPG18",
            "description": ""
        },
        {
            "id": "DOID:0110771",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110771",
            "name": "autosomal recessive spastic paraplegia 18",
            "description": ""
        },
        {
            "id": "DOID:0110771",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110771",
            "name": "autosomal recessive spastic paraplegia type 18",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "hereditary spastic paraplegia 18",
            "description": "gene (8p11.2) encoding the protein, Erlin-2."
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "autosomal recessive complex spastic paraplegia caused by mutation in ERLIN2",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "spastic paraplegia 18, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "autosomal recessive spastic paraplegia type 18",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "hereditary spastic paraplegia type 18",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "IDMDC",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "spastic paraplegia 18",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "intellectual disability, motor dysfunction and joint contractures",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "SPG18",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "spastic paraplegia 18, autosomal recessive; SPG18",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "ERLIN2 autosomal recessive complex spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "autosomal recessive spastic paraplegia 18",
            "description": ""
        },
        {
            "id": "MONDO:0012639",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012639",
            "name": "intellectual disability, motor dysfunction, and Joint contractures",
            "description": ""
        },
        {
            "id": "MIM:611225",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611225",
            "name": "Spastic paraplegia 18, autosomal recessive",
            "description": "Spastic paraplegia 18, autosomal recessive"
        }
    ]
}