{
    "disease_id": "DOID:0110815", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014303", 
            "name": "spastic paraplegia 64, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014303", 
            "name": "spastic paraplegia 64, autosomal recessive; SPG64"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014303", 
            "name": "hereditary spastic paraplegia type 64"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014303", 
            "name": "SPG64"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014303", 
            "name": "autosomal recessive spastic paraplegia type 64"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014303", 
            "name": "autosomal recessive complex spastic paraplegia caused by mutation in ENTPD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014303", 
            "name": "ENTPD1 autosomal recessive complex spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014303", 
            "name": "autosomal recessive spastic paraplegia 64"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110815", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110815", 
            "name": "SPG64"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110815", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110815", 
            "name": "autosomal recessive spastic paraplegia 64"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110815", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110815", 
            "name": "autosomal recessive spastic paraplegia type 64"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110815", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the ENTPD1 gene on chromosome 10q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110815", 
        "name": "hereditary spastic paraplegia 64"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110815#disease-associations", 
            "id": "0110815", 
            "database": "Alliance of Genome Resources"
        }
    ]
}