{
    "disease_id": "DOID:0110737",
    "recommended_name": {
        "id": "DOID:0110737",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110737",
        "name": "neurodegeneration with brain iron accumulation 3",
        "description": "A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal dominant inheritance of mutation in the FTL gene on chromosome 19q13.33."
    },
    "synonyms": [
        {
            "id": "DOID:0110737",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110737",
            "name": "Adult basal ganglia disease",
            "description": ""
        },
        {
            "id": "DOID:0110737",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110737",
            "name": "Ferritin-related neurodegeneration",
            "description": ""
        },
        {
            "id": "DOID:0110737",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110737",
            "name": "Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset",
            "description": ""
        },
        {
            "id": "DOID:0110737",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110737",
            "name": "Hereditary ferritinopathy",
            "description": ""
        },
        {
            "id": "DOID:0110737",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110737",
            "name": "NBIA3",
            "description": ""
        },
        {
            "id": "DOID:0110737",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110737",
            "name": "Neuroferritinopathy",
            "description": ""
        },
        {
            "id": "MONDO:0011638",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011638",
            "name": "neuroferritinopathy",
            "description": "Neuroferritinopathy is a late-onset type of neurodegeneration with brain iron accumulation (NBIA) characterized by progressive chorea or dystonia and subtle cognitive deficits."
        },
        {
            "id": "MONDO:0011638",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011638",
            "name": "NBIA3",
            "description": ""
        },
        {
            "id": "MONDO:0011638",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011638",
            "name": "adult basal ganglia disease",
            "description": ""
        },
        {
            "id": "MONDO:0011638",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011638",
            "name": "ferritin-related neurodegeneration",
            "description": ""
        },
        {
            "id": "MONDO:0011638",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011638",
            "name": "hereditary ferritinopathy",
            "description": ""
        },
        {
            "id": "MONDO:0011638",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011638",
            "name": "neurodegeneration with brain iron accumulation type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011638",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011638",
            "name": "neuroferritinopathy",
            "description": ""
        },
        {
            "id": "MONDO:0011638",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011638",
            "name": "basal ganglia disease adult-onset",
            "description": ""
        },
        {
            "id": "MONDO:0011638",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011638",
            "name": "neurodegeneration with brain iron accumulation 3",
            "description": ""
        },
        {
            "id": "MIM:606159",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/606159",
            "name": "Neurodegeneration with brain iron accumulation 3",
            "description": "Neurodegeneration with brain iron accumulation 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110737"
    ],
    "unlinked_id_list": []
}