{
    "disease_id": "DOID:0110817", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014282", 
            "name": "spastic paraplegia 72, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014282", 
            "name": "hereditary spastic paraplegia type 72"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014282", 
            "name": "spastic paraplegia 72, autosomal recessive; SPG72"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014282", 
            "name": "autosomal spastic paraplegia type 72"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014282", 
            "name": "pure hereditary spastic paraplegia caused by mutation in REEP2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014282", 
            "name": "SPG72"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014282", 
            "name": "REEP2 pure hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014282", 
            "name": "spastic paraplegia 72, autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110817", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110817", 
            "name": "SPG72"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110817", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110817", 
            "name": "autosomal spastic paraplegia type 72"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110817", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP2 gene on chromosome 5q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110817", 
        "name": "hereditary spastic paraplegia 72"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110817#disease-associations", 
            "id": "0110817", 
            "database": "Alliance of Genome Resources"
        }
    ]
}