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