{
    "disease_id": "DOID:0110802",
    "recommended_name": {
        "id": "DOID:0110802",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110802",
        "name": "hereditary spastic paraplegia 50",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4M1 gene on chromosome 7q22.1."
    },
    "synonyms": [
        {
            "id": "DOID:0110802",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110802",
            "name": "SPG50",
            "description": ""
        },
        {
            "id": "DOID:0110802",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110802",
            "name": "autosomal recessive spastic paraplegia 50",
            "description": ""
        },
        {
            "id": "DOID:0110802",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110802",
            "name": "AP-4 deficiency syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110802",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110802",
            "name": "AP-4-Associated Hereditary Spastic Paraplegia",
            "description": ""
        },
        {
            "id": "DOID:0110802",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110802",
            "name": "adaptor protein complex 4 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013048",
            "name": "hereditary spastic paraplegia 50",
            "description": "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4M1 gene."
        },
        {
            "id": "MONDO:0013048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013048",
            "name": "AP4M1 hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0013048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013048",
            "name": "SPG50",
            "description": ""
        },
        {
            "id": "MONDO:0013048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013048",
            "name": "Spastic Paraplegia 50",
            "description": ""
        },
        {
            "id": "MONDO:0013048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013048",
            "name": "hereditary spastic paraplegia caused by mutation in AP4M1",
            "description": ""
        },
        {
            "id": "MONDO:0013048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013048",
            "name": "hereditary spastic paraplegia type 50",
            "description": ""
        },
        {
            "id": "MONDO:0013048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013048",
            "name": "cerebral palsy, spastic quadriplegic, 3",
            "description": ""
        },
        {
            "id": "MONDO:0013048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013048",
            "name": "spastic paraplegia 50, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:612936",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612936",
            "name": "Spastic paraplegia 50, autosomal recessive",
            "description": "Spastic paraplegia 50, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110802"
    ],
    "unlinked_id_list": []
}