{
    "disease_id": "DOID:0110804", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "spastic paraplegia 52, autosomal recessive; SPG52"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "SPG52"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "hereditary spastic paraplegia caused by mutation in AP4S1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "hereditary spastic paraplegia type 52"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "cerebral palsy, spastic quadriplegic, 6, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "CPSQ6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "cerebral palsy, spastic quadriplegic, 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "autosomal recessive spastic paraplegia 52"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "spastic paraplegia 52, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "AP4S1 hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013552", 
            "name": "spastic quadriplegic cerebral palsy 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110804", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110804", 
            "name": "CPSQ6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110804", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110804", 
            "name": "SPG52"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110804", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110804", 
            "name": "autosomal recessive spastic paraplegia 52"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110804", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110804", 
            "name": "spastic quadriplegic cerebral palsy 6"
        }, 
        {
            "url": "https://www.omim.org/entry/614067", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614067", 
            "name": "Spastic paraplegia 52, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110804", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4S1 gene on chromosome 14q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110804", 
        "name": "hereditary spastic paraplegia 52"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614067", 
            "id": "614067", 
            "database": "MIM"
        }
    ]
}
