{
    "disease_id": "DOID:0061138",
    "recommended_name": {
        "id": "DOID:0061138",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061138",
        "name": "complex cortical dysplasia with other brain malformations 9",
        "description": "A complex cortical dysplasia with other brain malformations characterized by profoundly impaired motor and cognitive development apparent from early infancy that has_material_basis_in homozygous mutation in the CTNNA2 gene on chromosome 2p12."
    },
    "synonyms": [
        {
            "id": "DOID:0061138",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061138",
            "name": "CDCBM9",
            "description": ""
        },
        {
            "id": "MONDO:0032578",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032578",
            "name": "cortical dysplasia, complex, with other brain malformations 9",
            "description": ""
        },
        {
            "id": "MONDO:0032578",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032578",
            "name": "CDCBM9",
            "description": ""
        },
        {
            "id": "MIM:618174",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618174",
            "name": "Cortical dysplasia, complex, with other brain malformations 9",
            "description": "Cortical dysplasia, complex, with other brain malformations 9"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061138"
    ],
    "unlinked_id_list": []
}