{
    "disease_id": "DOID:0110818", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014568", 
            "name": "autosomal dominant spastic paraplegia 73"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014568", 
            "name": "autosomal dominant spastic paraplegia type 73"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014568", 
            "name": "hereditary spastic paraplegia type 73"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014568", 
            "name": "spastic paraplegia 73, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014568", 
            "name": "spastic paraplegia 73, autosomal dominant; SPG73"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014568", 
            "name": "SPG73"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014568", 
            "name": "CPT1C autosomal dominant pure spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014568", 
            "name": "autosomal dominant pure spastic paraplegia caused by mutation in CPT1C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110818", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110818", 
            "name": "SPG73"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110818", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110818", 
            "name": "autosomal dominant spastic paraplegia 73"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110818", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110818", 
            "name": "autosomal dominant spastic paraplegia type 73"
        }, 
        {
            "url": "https://www.omim.org/entry/616282", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616282", 
            "name": "Spastic paraplegia 73, autosomal dominant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110818", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the CPT1C gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110818", 
        "name": "hereditary spastic paraplegia 73"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616282", 
            "id": "616282", 
            "database": "MIM"
        }
    ]
}