{
    "disease_id": "DOID:0110771", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "autosomal recessive complex spastic paraplegia caused by mutation in ERLIN2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "spastic paraplegia 18, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "autosomal recessive spastic paraplegia type 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "hereditary spastic paraplegia type 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "IDMDC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "spastic paraplegia 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "intellectual disability, motor dysfunction and joint contractures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "SPG18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "spastic paraplegia 18, autosomal recessive; SPG18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "ERLIN2 autosomal recessive complex spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "autosomal recessive spastic paraplegia 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012639", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012639", 
            "name": "intellectual disability, motor dysfunction, and Joint contractures"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110771", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110771", 
            "name": "intellectual disability, motor dysfunction and joint contractures"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110771", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110771", 
            "name": "IDMDC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110771", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110771", 
            "name": "SPG18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110771", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110771", 
            "name": "autosomal recessive spastic paraplegia 18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110771", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110771", 
            "name": "autosomal recessive spastic paraplegia type 18"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110771", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110771", 
        "name": "hereditary spastic paraplegia 18"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110771#disease-associations", 
            "id": "0110771", 
            "database": "Alliance of Genome Resources"
        }
    ]
}