{
    "disease_id": "DOID:0112236",
    "recommended_name": {
        "id": "DOID:0112236",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112236",
        "name": "lissencephaly 6",
        "description": "A microlissencephaly characterized by severe microcephaly, developmental delay, lissencephaly, pachygyria, and hypoplasia of the corpus callosum that has_material_basis_in homozygous or compound heterozygous mutation in the KATNB1 gene on chromosome 16q21."
    },
    "synonyms": [
        {
            "id": "DOID:0112236",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112236",
            "name": "LIS6",
            "description": ""
        },
        {
            "id": "MONDO:0014534",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014534",
            "name": "lissencephaly 6 with microcephaly",
            "description": "Any microlissencephaly in which the cause of the disease is a mutation in the KATNB1 gene."
        },
        {
            "id": "MONDO:0014534",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014534",
            "name": "KATNB1 Microlissencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0014534",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014534",
            "name": "KATNB1 microlissencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0014534",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014534",
            "name": "Microlissencephaly caused by mutation in KATNB1",
            "description": ""
        },
        {
            "id": "MONDO:0014534",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014534",
            "name": "lissencephaly 6 with microcephaly",
            "description": ""
        },
        {
            "id": "MONDO:0014534",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014534",
            "name": "lissencephaly 6, with microcephaly",
            "description": ""
        },
        {
            "id": "MONDO:0014534",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014534",
            "name": "microlissencephaly caused by mutation in KATNB1",
            "description": ""
        },
        {
            "id": "MONDO:0014534",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014534",
            "name": "LIS6",
            "description": ""
        },
        {
            "id": "MIM:616212",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616212",
            "name": "Lissencephaly 6, with microcephaly",
            "description": "Lissencephaly 6, with microcephaly"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112236"
    ],
    "unlinked_id_list": []
}