{
    "disease_id": "DOID:0110824", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011006", 
            "description": "", 
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            "description": "", 
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        {
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011006", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011006", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "AD-SPG9A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011006", 
            "description": "", 
            "resource": "MONDO", 
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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011006", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011006", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011006", 
            "name": "spastic paraplegia 9A, autosomal dominant; SPG9A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011006", 
            "name": "spastic paraplegia 9A, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011006", 
            "name": "spastic paraparesis with amyopathy, cataracts, and gastroesophageal reflux"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110824", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110824", 
            "name": "cataracts with motor neuronopathy, short stature and skeletal abnormalities"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110824", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110824", 
            "name": "AD-SPG9A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110824", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110824", 
            "name": "SPG9A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110824", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110824", 
            "name": "autosomal dominant spastic paraplegia 9A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110824", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110824", 
            "name": "spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110824", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110824", 
            "name": "Cataracts motor neuropathy-short stature-skeletal anomalies syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110824", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110824", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110824", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110824", 
            "name": "autosomal dominant complex spastic paraplegia type 9A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110824", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in autosomal dominant heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110824", 
        "name": "hereditary spastic paraplegia 9A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110824#disease-associations", 
            "id": "0110824", 
            "database": "Alliance of Genome Resources"
        }
    ]
}