{
    "disease_id": "DOID:0110790", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012787", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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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": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012787", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "spastic paraplegia 39, autosomal recessive"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012787", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012787", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012787", 
            "name": "spastic paraplegia due to neuropathy target esterase mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012787", 
            "name": "spastic paraplegia 39, autosomal recessive; SPG39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012787", 
            "name": "NTEMND"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012787", 
            "name": "autosomal recessive spastic paraplegia type 39"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110790", 
            "name": "NTE-related motor neuron disorder"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110790", 
            "name": "NTEMND"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110790", 
            "name": "SPG39"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110790", 
            "name": "spastic paraplegia due to neuropathy target esterase mutation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110790", 
            "name": "autosomal recessive spastic paraplegia 39"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110790", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110790", 
            "name": "spastic paraplegia due to NTE mutation"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110790", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the PNPLA6 gene on chromosome 19p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110790", 
        "name": "hereditary spastic paraplegia 39"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110790#disease-associations", 
            "id": "0110790", 
            "database": "Alliance of Genome Resources"
        }
    ]
}