{
    "disease_id": "DOID:0110801",
    "recommended_name": {
        "id": "DOID:0110801",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110801",
        "name": "hereditary spastic paraplegia 49",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32."
    },
    "synonyms": [
        {
            "id": "DOID:0110801",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110801",
            "name": "SPG49",
            "description": ""
        },
        {
            "id": "DOID:0110801",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110801",
            "name": "autosomal recessive spastic paraplegia 49",
            "description": ""
        },
        {
            "id": "DOID:0110801",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110801",
            "name": "autosomal recessive spastic paraplegia type 49",
            "description": ""
        },
        {
            "id": "MONDO:0014016",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014016",
            "name": "hereditary spastic paraplegia 49",
            "description": "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the TECPR2 gene."
        },
        {
            "id": "MONDO:0014016",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014016",
            "name": "SPG49",
            "description": ""
        },
        {
            "id": "MONDO:0014016",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014016",
            "name": "TECPR2 hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0014016",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014016",
            "name": "autosomal recessive spastic paraplegia 49",
            "description": ""
        },
        {
            "id": "MONDO:0014016",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014016",
            "name": "autosomal recessive spastic paraplegia type 49",
            "description": ""
        },
        {
            "id": "MONDO:0014016",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014016",
            "name": "hereditary spastic paraplegia 49",
            "description": ""
        },
        {
            "id": "MONDO:0014016",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014016",
            "name": "hereditary spastic paraplegia caused by mutation in TECPR2",
            "description": ""
        },
        {
            "id": "MONDO:0014016",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014016",
            "name": "hereditary spastic paraplegia type 49",
            "description": ""
        },
        {
            "id": "MONDO:0014016",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014016",
            "name": "neuropathy, hereditary sensory and autonomic, type IX, with developmental delay",
            "description": ""
        },
        {
            "id": "MONDO:0014016",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014016",
            "name": "spastic paraplegia 49, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:615031",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615031",
            "name": "Neuropathy, hereditary sensory and autonomic, 9, with developmental delay",
            "description": "Neuropathy, hereditary sensory and autonomic, 9, with developmental delay"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110801"
    ],
    "unlinked_id_list": []
}