{
    "disease_id": "DOID:0112233",
    "recommended_name": {
        "id": "DOID:0112233",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112233",
        "name": "lissencephaly 8",
        "description": "A lissencephaly characterized by delayed psychomotor development, intellectual disability with poor or absent speech, early-onset refractory seizures, and hypotonia that has_material_basis_in homozygous or compound heterozygous mutation in the TMTC3 gene on chromosome 12q21.32."
    },
    "synonyms": [
        {
            "id": "DOID:0112233",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112233",
            "name": "LIS8",
            "description": ""
        },
        {
            "id": "MONDO:0014992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014992",
            "name": "lissencephaly 8",
            "description": "Any lissencephaly (disease) in which the cause of the disease is a mutation in the TMTC3 gene."
        },
        {
            "id": "MONDO:0014992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014992",
            "name": "LIS8",
            "description": ""
        },
        {
            "id": "MONDO:0014992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014992",
            "name": "TMTC3 lissencephaly (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0014992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014992",
            "name": "lissencephaly (disease) caused by mutation in TMTC3",
            "description": ""
        },
        {
            "id": "MONDO:0014992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014992",
            "name": "lissencephaly 8",
            "description": ""
        },
        {
            "id": "MONDO:0014992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014992",
            "name": "lissencephaly 8; LIS8",
            "description": ""
        },
        {
            "id": "MONDO:0014992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014992",
            "name": "lissencephaly type 8",
            "description": ""
        },
        {
            "id": "MIM:617255",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617255",
            "name": "Lissencephaly 8",
            "description": "Lissencephaly 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112233"
    ],
    "unlinked_id_list": []
}