{
    "disease_id": "DOID:0111450", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014685", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014685", 
            "name": "progressive myoclonic epilepsy type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014685", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014685", 
            "name": "PME type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014685", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014685", 
            "name": "EPM9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014685", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014685", 
            "name": "LMNB2 progressive myoclonic epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014685", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014685", 
            "name": "progressive myoclonus epilepsy type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014685", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014685", 
            "name": "epilepsy, progressive myoclonic, type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014685", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014685", 
            "name": "progressive myoclonic epilepsy due to LMNB2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014685", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014685", 
            "name": "progressive myoclonic epilepsy caused by mutation in LMNB2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014685", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014685", 
            "name": "epilepsy, progressive myoclonic, 9; EPM9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014685", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014685", 
            "name": "epilepsy, progressive myoclonic, 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111450", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111450", 
            "name": "EMP9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111450", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111450", 
            "name": "PME type 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111450", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111450", 
            "name": "progressive myoclonus epilepsy type 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111450", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111450", 
            "name": "progressive myoclonic epilepsy due to LMNB2 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111450", 
        "description": "A progressive myoclonus epilepsy characterized by childhood-onset severe myoclonic and tonic-clonic seizures and early-onset ataxia that has_material_basis_in homozygous or compound heterozygous mutation in LMNB2 on chromosome 19p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111450", 
        "name": "progressive myoclonus epilepsy 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111450#disease-associations", 
            "id": "0111450", 
            "database": "Alliance of Genome Resources"
        }
    ]
}