{
    "disease_id": "DOID:0080923",
    "recommended_name": {
        "id": "DOID:0080923",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080923",
        "name": "bilateral parasagittal parieto-occipital polymicrogyria",
        "description": "A polymicrogyria that is characterized by bilateral malformation of cortical development, centered around the parasagittal and mesial aspects of the parietooccipital cortex and that has_material_basis_in homozygous mutation in the FIG4 gene on chromosome 6q21."
    },
    "synonyms": [
        {
            "id": "DOID:0080923",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080923",
            "name": "bilateral temporooccipital polymicrogyria",
            "description": ""
        },
        {
            "id": "MONDO:0012986",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012986",
            "name": "bilateral parasagittal parieto-occipital polymicrogyria",
            "description": ""
        },
        {
            "id": "MONDO:0012986",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012986",
            "name": "BTOP",
            "description": ""
        },
        {
            "id": "MONDO:0012986",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012986",
            "name": "polymicrogyria, bilateral temporooccipital",
            "description": ""
        },
        {
            "id": "MIM:612691",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612691",
            "name": "Polymicrogyria, bilateral temporooccipital",
            "description": "Polymicrogyria, bilateral temporooccipital"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080923"
    ],
    "unlinked_id_list": []
}