{
    "disease_id": "DOID:0110736", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012444", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012444", 
            "name": "neurodegeneration with brain iron accumulation type 2b"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012444", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012444", 
            "name": "neurodegeneration with brain iron accumulation, Pla2g6-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012444", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012444", 
            "name": "neurodegeneration with brain iron accumulation 2B; NBIA2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012444", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012444", 
            "name": "Karak syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012444", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012444", 
            "name": "atypical neuroaxonal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012444", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012444", 
            "name": "NBIA2b"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012444", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012444", 
            "name": "early-onset progressive cerebellar ataxia dystonia spasticity and intellectual decline"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012444", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012444", 
            "name": "neuroaxonal dystrophy, atypical"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110736", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110736", 
            "name": "NBIA2b"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110736", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110736", 
            "name": "Neuroaxonal Dystrophy, Atypical"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110736", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110736", 
            "name": "Neurodegeneration With Brain Iron Accumulation, Pla2g6-Related"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110736", 
        "description": "A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PLA2G6 gene on chromosome 22q13.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110736", 
        "name": "neurodegeneration with brain iron accumulation 2b"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610217", 
            "id": "610217", 
            "database": "MIM"
        }
    ]
}