{
    "disease_id": "DOID:0110737", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011638", 
            "name": "neuroferritinopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011638", 
            "name": "neurodegeneration with brain iron accumulation 3; NBIA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011638", 
            "name": "hereditary ferritinopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011638", 
            "name": "neurodegeneration with brain iron accumulation type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011638", 
            "name": "basal ganglia disease adult-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011638", 
            "name": "Neuroferritinopathy; basal ganglia disease, adult-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011638", 
            "name": "adult basal ganglia disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011638", 
            "name": "basal ganglia disease, adult-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011638", 
            "name": "ferritin-related neurodegeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011638", 
            "name": "NBIA3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110737", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110737", 
            "name": "Adult basal ganglia disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110737", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110737", 
            "name": "Ferritin-related neurodegeneration"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110737", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110737", 
            "name": "Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110737", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110737", 
            "name": "Hereditary ferritinopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110737", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110737", 
            "name": "NBIA3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110737", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110737", 
            "name": "Neuroferritinopathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110737", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110737", 
        "name": "neurodegeneration with brain iron accumulation 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110737#disease-associations", 
            "id": "0110737", 
            "database": "Alliance of Genome Resources"
        }
    ]
}