{
    "disease_id": "DOID:0110812",
    "recommended_name": {
        "id": "DOID:0110812",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110812",
        "name": "hereditary spastic paraplegia 61",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12."
    },
    "synonyms": [
        {
            "id": "DOID:0110812",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110812",
            "name": "SPG61",
            "description": ""
        },
        {
            "id": "DOID:0110812",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110812",
            "name": "autosomal recessive spastic paraplegia 61",
            "description": ""
        },
        {
            "id": "DOID:0110812",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110812",
            "name": "autosomal recessive spastic paraplegia type 61",
            "description": ""
        },
        {
            "id": "MONDO:0014304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014304",
            "name": "hereditary spastic paraplegia 61",
            "description": "A rare, complex form of hereditary spastic paraplegia characterized by an onset in infancy of spastic paraplegia (presenting with the inability to walk unsupported and a scissors gait) associated with a motor and sensory polyneuropathy with loss of terminal digits and acropathy. SPG61 is due to a mutation in the ARL6IP1 gene (16p12-p11.2) encoding the ADP-ribosylation factor-like protein 6-interacting protein 1."
        },
        {
            "id": "MONDO:0014304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014304",
            "name": "ARL6IP1 autosomal recessive complex spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0014304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014304",
            "name": "SPG61",
            "description": ""
        },
        {
            "id": "MONDO:0014304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014304",
            "name": "autosomal recessive complex spastic paraplegia caused by mutation in ARL6IP1",
            "description": ""
        },
        {
            "id": "MONDO:0014304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014304",
            "name": "autosomal recessive spastic paraplegia type 61",
            "description": ""
        },
        {
            "id": "MONDO:0014304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014304",
            "name": "hereditary spastic paraplegia 61",
            "description": ""
        },
        {
            "id": "MONDO:0014304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014304",
            "name": "hereditary spastic paraplegia type 61",
            "description": ""
        },
        {
            "id": "MONDO:0014304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014304",
            "name": "spastic paraplegia 61, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:615685",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615685",
            "name": "Spastic paraplegia 61, autosomal recessive",
            "description": "Spastic paraplegia 61, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110812"
    ],
    "unlinked_id_list": []
}