{
    "disease_id": "DOID:0061246",
    "recommended_name": {
        "id": "DOID:0061246",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061246",
        "name": "periventricular nodular heterotopia 9",
        "description": "A periventricular nodular heterotopia characterized as a malformation of cortical development that has_material_basis_in heterozygous mutation in the MAP1B gene on chromosome 5q13."
    },
    "synonyms": [
        {
            "id": "MONDO:0030061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030061",
            "name": "periventricular nodular heterotopia 9",
            "description": ""
        },
        {
            "id": "MONDO:0030061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030061",
            "name": "PERIVENTRICULAR NODULAR HETEROTOPIA 9",
            "description": ""
        },
        {
            "id": "MONDO:0030061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030061",
            "name": "PVNH9",
            "description": ""
        },
        {
            "id": "MONDO:0030061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030061",
            "name": "periventricular nodular heterotopia 9",
            "description": ""
        },
        {
            "id": "MIM:618918",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618918",
            "name": "Periventricular nodular heterotopia 9",
            "description": "Periventricular nodular heterotopia 9"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061246"
    ],
    "unlinked_id_list": []
}