{
    "disease_id": "DOID:0110765",
    "recommended_name": {
        "id": "DOID:0110765",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110765",
        "name": "hereditary spastic paraplegia 12",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110765",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110765",
            "name": "SPG12",
            "description": ""
        },
        {
            "id": "DOID:0110765",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110765",
            "name": "autosomal dominant spastic paraplegia 12",
            "description": ""
        },
        {
            "id": "DOID:0110765",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110765",
            "name": "autosomal dominant spastic paraplegia type 12",
            "description": ""
        },
        {
            "id": "MONDO:0011489",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011489",
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            "description": "Autosomal dominant spastic paraplegia type 12 is a pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus."
        },
        {
            "id": "MONDO:0011489",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011489",
            "name": "RTN2 hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0011489",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011489",
            "name": "SPG12",
            "description": ""
        },
        {
            "id": "MONDO:0011489",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011489",
            "name": "autosomal dominant spastic paraplegia type 12",
            "description": ""
        },
        {
            "id": "MONDO:0011489",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011489",
            "name": "hereditary spastic paraplegia caused by mutation in RTN2",
            "description": ""
        },
        {
            "id": "MONDO:0011489",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011489",
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            "description": ""
        },
        {
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            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011489",
            "name": "spastic paraplegia 12",
            "description": ""
        },
        {
            "id": "MONDO:0011489",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011489",
            "name": "spastic paraplegia 12, autosomal dominant",
            "description": ""
        },
        {
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            "resource": "MIM",
            "url": "https://www.omim.org/entry/604805",
            "name": "Spastic paraplegia 12, autosomal dominant",
            "description": "Spastic paraplegia 12, autosomal dominant"
        }
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    "id_list": [
        "DOID:0110765"
    ],
    "unlinked_id_list": [],
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            "id": "DOID:0110765",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110765",
            "categories": []
        },
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            "url": "https://monarchinitiative.org/disease/MONDO:0011489",
            "categories": []
        },
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            "url": "https://www.omim.org/entry/604805",
            "categories": []
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    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0110765"
}