{
    "disease_id": "DOID:0061245",
    "recommended_name": {
        "id": "DOID:0061245",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061245",
        "name": "periventricular nodular heterotopia 8",
        "description": "A periventricular nodular heterotopia characterized by abnormal neuronal migration during brain development, resulting in delayed psychomotor development that has_material_basis_in heterozygous mutation in the ARF1 gene on chromosome 1q42."
    },
    "synonyms": [
        {
            "id": "MONDO:0032588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032588",
            "name": "periventricular nodular heterotopia 8",
            "description": ""
        },
        {
            "id": "MONDO:0032588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032588",
            "name": "PVNH8",
            "description": ""
        },
        {
            "id": "MIM:618185",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618185",
            "name": "Periventricular nodular heterotopia 8",
            "description": "Periventricular nodular heterotopia 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061245"
    ],
    "unlinked_id_list": []
}