{
    "disease_id": "DOID:0110800", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013342", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "autosomal recessive spastic paraplegia type 48"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013342", 
            "name": "spastic paraplegia 48, autosomal recessive; SPG48"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "spastic paraplegia 48, autosomal recessive"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "hereditary spastic paraplegia type 48"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013342", 
            "name": "autosomal recessive spastic paraplegia 48"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013342", 
            "name": "SPG48"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013342", 
            "name": "AP5Z1 hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013342", 
            "name": "hereditary spastic paraplegia caused by mutation in AP5Z1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110800", 
            "name": "SPG48"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110800", 
            "name": "autosomal recessive spastic paraplegia 48"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110800", 
            "name": "autosomal recessive spastic paraplegia type 48"
        }, 
        {
            "url": "https://www.omim.org/entry/613647", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613647", 
            "name": "Spastic paraplegia 48, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110800", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the AP5Z1 gene on chromosome 7p22.1.", 
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        "id": "DOID:0110800", 
        "name": "hereditary spastic paraplegia 48"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613647", 
            "id": "613647", 
            "database": "MIM"
        }
    ]
}