{
    "disease_id": "DOID:3981", 
    "synonyms": [
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009319", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009319", 
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        }, 
        {
            "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", 
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        }, 
        {
            "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:3981", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3981", 
            "name": "Hallervorden-Spatz disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3981", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3981", 
            "name": "Hallervorden-Spatz syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3981", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3981", 
            "name": "NBIA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3981", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3981", 
            "name": "Pigmentary pallidal degeneration"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3981", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3981", 
            "name": "brain Iron Accumulation type I syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3981", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3981", 
            "name": "neurodegeneration with brain iron accumulation 1"
        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:234200", 
            "name": "Neurodegeneration with brain iron accumulation 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3981", 
        "description": "A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:3981", 
        "name": "pantothenate kinase-associated neurodegeneration"
    }, 
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            "id": "234200", 
            "database": "MIM"
        }
    ]
}