{
    "disease_id": "DOID:0110768",
    "recommended_name": {
        "id": "DOID:0110768",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110768",
        "name": "hereditary spastic paraplegia 15",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1."
    },
    "synonyms": [
        {
            "id": "DOID:0110768",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110768",
            "name": "Kjellin syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110768",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110768",
            "name": "SPG15",
            "description": ""
        },
        {
            "id": "DOID:0110768",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110768",
            "name": "autosomal recessive spastic paraplegia 15",
            "description": ""
        },
        {
            "id": "DOID:0110768",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110768",
            "name": "autosomal recessive spastic paraplegia type 15",
            "description": ""
        },
        {
            "id": "DOID:0110768",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110768",
            "name": "hereditary spastic paraparesis type 15",
            "description": ""
        },
        {
            "id": "DOID:0110768",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110768",
            "name": "spastic paraplegia and retinal degeneration",
            "description": ""
        },
        {
            "id": "DOID:0110768",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110768",
            "name": "spastic paraplegia-retinal degeneration syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "hereditary spastic paraplegia 15",
            "description": "Autosomal recessive spastic paraplegia type 15 is a complex form of hereditary spastic paraplegia characterized by a childhood to adulthood onset of slowly progressive lower limb spasticity (resulting in gait disturbance, extensor plantar responses and decreased vibration sense) associated with mild intellectual disability, mild cerebellar ataxia, peripheral neuropathy (with distal upper limb amyotrophy) and retinal degeneration. Thin corpus callosum is a common imaging finding."
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "Kjellin syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "SPG15",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "ZFYVE26 autosomal recessive complex spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "autosomal recessive complex spastic paraplegia caused by mutation in ZFYVE26",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "autosomal recessive spastic paraplegia type 15",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "hereditary spastic paraparesis type 15",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "hereditary spastic paraplegia 15",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "hereditary spastic paraplegia type 15",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "spastic paraplegia and retinal degeneration",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "spastic paraplegia-retinal degeneration syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "recessive spastic paraplegia with retinal degeneration",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "spastic paraplegia 15",
            "description": ""
        },
        {
            "id": "MONDO:0010044",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010044",
            "name": "spastic paraplegia 15, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:270700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/270700",
            "name": "Spastic paraplegia 15, autosomal recessive",
            "description": "Spastic paraplegia 15, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110768"
    ],
    "unlinked_id_list": []
}