{
    "disease_id": "DOID:0110817",
    "recommended_name": {
        "id": "DOID:0110817",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110817",
        "name": "hereditary spastic paraplegia 72A",
        "description": "A hereditary spastic paraplegia that has_material_basis_in a heterozygous mutation in the REEP2 gene on chromosome 5q31.2."
    },
    "synonyms": [
        {
            "id": "DOID:0110817",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110817",
            "name": "SPG72",
            "description": ""
        },
        {
            "id": "MONDO:0014282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014282",
            "name": "hereditary spastic paraplegia 72",
            "description": "Any pure hereditary spastic paraplegia in which the cause of the disease is a mutation in the REEP2 gene."
        },
        {
            "id": "MONDO:0014282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014282",
            "name": "REEP2 pure hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0014282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014282",
            "name": "SPG72",
            "description": ""
        },
        {
            "id": "MONDO:0014282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014282",
            "name": "autosomal spastic paraplegia type 72",
            "description": ""
        },
        {
            "id": "MONDO:0014282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014282",
            "name": "hereditary spastic paraplegia type 72",
            "description": ""
        },
        {
            "id": "MONDO:0014282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014282",
            "name": "pure hereditary spastic paraplegia caused by mutation in REEP2",
            "description": ""
        },
        {
            "id": "MONDO:0014282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014282",
            "name": "spastic paraplegia 72, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0014282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014282",
            "name": "spastic paraplegia 72, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:615625",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615625",
            "name": "Spastic paraplegia 72A, autosomal dominant",
            "description": "Spastic paraplegia 72A, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110817"
    ],
    "unlinked_id_list": []
}