{
    "disease_id": "DOID:0112235",
    "recommended_name": {
        "id": "DOID:0112235",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112235",
        "name": "lissencephaly 4",
        "description": "A microlissencephaly characterized by lissencephaly, severe brain atrophy, extreme microcephaly, and profound intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in the NDE1 gene on chromosome 16p13.11."
    },
    "synonyms": [
        {
            "id": "DOID:0112235",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112235",
            "name": "LIS4",
            "description": ""
        },
        {
            "id": "DOID:0112235",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112235",
            "name": "lissencephaly 4 with microcephaly",
            "description": ""
        },
        {
            "id": "MONDO:0013527",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013527",
            "name": "lissencephaly 4",
            "description": "Any lissencephaly in which the cause of the disease is a mutation in the NDE1 gene."
        },
        {
            "id": "MONDO:0013527",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013527",
            "name": "NDE1 lissencephaly (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0013527",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013527",
            "name": "lissencephaly (disease) caused by mutation in NDE1",
            "description": ""
        },
        {
            "id": "MONDO:0013527",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013527",
            "name": "lissencephaly 4",
            "description": ""
        },
        {
            "id": "MONDO:0013527",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013527",
            "name": "lissencephaly 4 (with microcephaly)",
            "description": ""
        },
        {
            "id": "MONDO:0013527",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013527",
            "name": "lissencephaly type 4",
            "description": ""
        },
        {
            "id": "MONDO:0013527",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013527",
            "name": "LIS4",
            "description": ""
        },
        {
            "id": "MONDO:0013527",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013527",
            "name": "lissencephaly 4 with microcephaly",
            "description": ""
        },
        {
            "id": "MONDO:0013527",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013527",
            "name": "lissencephaly 4, with microcephaly",
            "description": ""
        },
        {
            "id": "MIM:614019",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614019",
            "name": "Lissencephaly 4 with microcephaly",
            "description": "Lissencephaly 4 with microcephaly"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112235"
    ],
    "unlinked_id_list": []
}