{
    "disease_id": "DOID:0110783",
    "recommended_name": {
        "id": "DOID:0110783",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110783",
        "name": "hereditary spastic paraplegia 32",
        "description": "A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110783",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110783",
            "name": "SPG32",
            "description": ""
        },
        {
            "id": "DOID:0110783",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110783",
            "name": "autosomal recessive spastic paraplegia 32",
            "description": ""
        },
        {
            "id": "DOID:0110783",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110783",
            "name": "autosomal recessive spastic paraplegia type 32",
            "description": ""
        },
        {
            "id": "MONDO:0012643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012643",
            "name": "hereditary spastic paraplegia 32",
            "description": "Autosomal recessive spastic paraplegia type 32 (SPG32) is a rare, complex type of hereditary spastic paraplegia characterized by a slowly progressive spastic paraplegia (with walking difficulties appearing at onset at 6-7 years of age) associated with mild intellectual disability. Brain imaging reveals thin corpus callosum, cortical and cerebellar atrophy, and pontine dysraphia. The SPG32 phenotype has been mapped to a locus on chromosome 14q12-q21."
        },
        {
            "id": "MONDO:0012643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012643",
            "name": "spastic paraplegia 32, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0012643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012643",
            "name": "SPG32",
            "description": ""
        },
        {
            "id": "MONDO:0012643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012643",
            "name": "spastic paraplegia 32",
            "description": ""
        },
        {
            "id": "MONDO:0012643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012643",
            "name": "hereditary spastic paraplegia type 32",
            "description": ""
        },
        {
            "id": "MONDO:0012643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012643",
            "name": "autosomal recessive spastic paraplegia type 32",
            "description": ""
        },
        {
            "id": "MONDO:0012643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012643",
            "name": "spastic paraplegia 32, autosomal recessive; SPG32",
            "description": ""
        },
        {
            "id": "MONDO:0012643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012643",
            "name": "autosomal recessive spastic paraplegia 32",
            "description": ""
        }
    ]
}