{
    "disease_id": "DOID:0111448", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012904", 
            "name": "epilepsy, progressive myoclonic, 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012904", 
            "name": "epilepsy, progressive myoclonic, 1B; EPM1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012904", 
            "name": "epilepsy, progressive myoclonic, type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012904", 
            "name": "PRICKLE1 progressive myoclonic epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012904", 
            "name": "progressive myoclonic epilepsy caused by mutation in PRICKLE1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012904", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012904", 
            "name": "EPM1B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111448", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111448", 
            "name": "EPM1B"
        }, 
        {
            "url": "https://www.omim.org/entry/612437", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:612437", 
            "name": "Epilepsy, progressive myoclonic 1B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111448", 
        "description": "An Unverricht-Lundborg syndrome that has_material_basis_in homozygous or compound heterozygous mutation in PRICKLE1 on chromosome 12q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111448", 
        "name": "progressive myoclonus epilepsy 1B"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612437", 
            "id": "612437", 
            "database": "MIM"
        }
    ]
}