{
    "disease_id": "DOID:0110810", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "spastic paraplegia 5A, autosomal recessive; SPG5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "spastic paraplegia type 5B, recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "hereditary spastic paraplegia type 5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "CYP7B1 pure or complex autosomal recessive spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "spastic paraplegia type 5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "spastic paraplegia 5A, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "autosomal recessive spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "autosomal recessive spastic paraplegia type 5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "pure or complex autosomal recessive spastic paraplegia caused by mutation in CYP7B1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "spastic paraplegia 5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "autosomal recessive spastic paraplegia 5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010047", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010047", 
            "name": "SPG5A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110810", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110810", 
            "name": "SPG5A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110810", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110810", 
            "name": "autosomal recessive spastic paraplegia 5A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110810", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110810", 
            "name": "autosomal recessive spastic paraplegia type 5A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110810", 
        "description": "A hereditary spastic paraplegia that is characterized by progressive muscle weakness and paraplegia and has_material_basis_in mutation in the CYP7B1 gene on chromosome 8q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110810", 
        "name": "hereditary spastic paraplegia 5A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110810#disease-associations", 
            "id": "0110810", 
            "database": "Alliance of Genome Resources"
        }
    ]
}