{
    "disease_id": "DOID:0110808",
    "recommended_name": {
        "id": "DOID:0110808",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110808",
        "name": "hereditary spastic paraplegia 56",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25."
    },
    "synonyms": [
        {
            "id": "DOID:0110808",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110808",
            "name": "SPG56",
            "description": ""
        },
        {
            "id": "DOID:0110808",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110808",
            "name": "autosomal recessive spastic paraplegia 56",
            "description": ""
        },
        {
            "id": "DOID:0110808",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110808",
            "name": "autosomal recessive spastic paraplegia type 56",
            "description": ""
        },
        {
            "id": "MONDO:0014015",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014015",
            "name": "hereditary spastic paraplegia 56",
            "description": "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the CYP2U1 gene."
        },
        {
            "id": "MONDO:0014015",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014015",
            "name": "autosomal recessive spastic paraplegia 56",
            "description": ""
        },
        {
            "id": "MONDO:0014015",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014015",
            "name": "spastic paraplegia 56, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0014015",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014015",
            "name": "hereditary spastic paraplegia caused by mutation in CYP2U1",
            "description": ""
        },
        {
            "id": "MONDO:0014015",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014015",
            "name": "CYP2U1 hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0014015",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014015",
            "name": "SPG56",
            "description": ""
        },
        {
            "id": "MONDO:0014015",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014015",
            "name": "spastic paraplegia 56, autosomal recessive; SPG56",
            "description": ""
        },
        {
            "id": "MONDO:0014015",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014015",
            "name": "autosomal recessive spastic paraplegia type 56",
            "description": ""
        },
        {
            "id": "MONDO:0014015",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014015",
            "name": "hereditary spastic paraplegia type 56",
            "description": ""
        },
        {
            "id": "MIM:615030",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615030",
            "name": "Spastic paraplegia 56, autosomal recessive",
            "description": "Spastic paraplegia 56, autosomal recessive"
        }
    ]
}