{
    "disease_id": "DOID:0110734", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "pantothenate kinase-associated neurodegeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "neuroaxonal dystrophy, late infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "pigmentary pallidal degeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "NBIA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "neurodegeneration with brain iron accumulation type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "PKAN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "neurodegeneration with brain iron accumulation 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "Hallervorden-Spatz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "brain iron accumulation type I syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "Hallervorden-Spatz disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "neurodegeneration with brain iron accumulation 1; NBIA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
            "name": "Pkan neuroaxonal dystrophy, juvenile-onset"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110734", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110734", 
            "name": "NBIA"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110734", 
        "description": "A neurodegenerative disease characterized by progressive iron accumulation in the basal ganglia and other regions of the brain, resulting in extrapyramidal movements, such as parkinsonism and dystonia.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110734", 
        "name": "neurodegeneration with brain iron accumulation"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110734#disease-associations", 
            "id": "0110734", 
            "database": "Alliance of Genome Resources"
        }
    ]
}