{
    "disease_id": "DOID:0061270",
    "recommended_name": {
        "id": "DOID:0061270",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061270",
        "name": "periventricular nodular heterotopia 7",
        "description": "A periventricular nodular heterotopia characterized by abnormal neuronal migration during brain development resulting in delayed psychomotor development and intellectual disability; some patients develop seizures that has_material_basis_in heterozygous mutation in the NEDD4L gene on chromosome 18q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0014966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014966",
            "name": "periventricular nodular heterotopia 7",
            "description": "Any periventricular nodular heterotopia in which the cause of the disease is a mutation in the NEDD4L gene."
        },
        {
            "id": "MONDO:0014966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014966",
            "name": "NEDD4L periventricular nodular heterotopia",
            "description": ""
        },
        {
            "id": "MONDO:0014966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014966",
            "name": "PVNH7",
            "description": ""
        },
        {
            "id": "MONDO:0014966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014966",
            "name": "periventricular nodular heterotopia 7",
            "description": ""
        },
        {
            "id": "MONDO:0014966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014966",
            "name": "periventricular nodular heterotopia 7; PVNH7",
            "description": ""
        },
        {
            "id": "MONDO:0014966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014966",
            "name": "periventricular nodular heterotopia caused by mutation in NEDD4L",
            "description": ""
        },
        {
            "id": "MONDO:0014966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014966",
            "name": "periventricular nodular heterotopia type 7",
            "description": ""
        },
        {
            "id": "MIM:617201",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617201",
            "name": "Periventricular nodular heterotopia 7",
            "description": "Periventricular nodular heterotopia 7"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061270"
    ],
    "unlinked_id_list": []
}