{
    "disease_id": "DOID:0080924",
    "recommended_name": {
        "id": "DOID:0080924",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080924",
        "name": "bilateral perisylvian polymicrogyria",
        "description": "A polymicrogyria that is characterized by strikingly restricted polymicrogyria limited to the cortex surrounding the Sylvian fissure and that has_material_basis_in homozygous deletion of one 15-bp tandem repeat in a regulatory region of exon 1m of the ADGRG1 gene on chromosome 16q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0014333",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014333",
            "name": "polymicrogyria, bilateral perisylvian, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0014333",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014333",
            "name": "polymicrogyria, bilateral perisylvian",
            "description": ""
        },
        {
            "id": "MONDO:0014333",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014333",
            "name": "polymicrogyria, bilateral perisylvian, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0014333",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014333",
            "name": "BPPR",
            "description": ""
        },
        {
            "id": "MONDO:0014333",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014333",
            "name": "Pmgr",
            "description": ""
        },
        {
            "id": "MIM:615752",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615752",
            "name": "Polymicrogyria, bilateral perisylvian, autosomal recessive",
            "description": "Polymicrogyria, bilateral perisylvian, autosomal recessive"
        }
    ]
}