{
    "disease_id": "DOID:0112239",
    "recommended_name": {
        "id": "DOID:0112239",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112239",
        "name": "X-linked lissencephaly 1",
        "description": "A lissencephaly characterized by classic lissencephaly and intellectual disability in males that has_material_basis_in mutation in DCX on chromosome Xq23."
    },
    "synonyms": [
        {
            "id": "DOID:0112239",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112239",
            "name": "XLIS1",
            "description": ""
        },
        {
            "id": "DOID:0112239",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112239",
            "name": "lissencephaly type 1 due to doublecortin gene mutation",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "lissencephaly type 1 due to doublecortin gene mutation",
            "description": "Type 1 lissencephaly due to doublecortin (DCX) gene mutations is a semi-dominant X-linked disease characterized by intellectual deficiency and seizures that are more severe in male patients."
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "X-linked lissencephaly type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "lissencephaly type 1 due to doublecortin gene mutation",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "lissencephaly, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "lissencephaly, X-linked, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "subcortical laminal heterotopia, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "Dc syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "Double cortex syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "LISX",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "LISX1",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "X-linked lissencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "XLIS",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "Xlis",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "lissencephaly X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "lissencephaly and agenesis of corpus callosum",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "lissencephaly, X-linked, 1",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "subcortical band heterotopia, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "subcortical laminar heterotopia, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010239",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010239",
            "name": "subcortical laminar heterotopia, X-linked,",
            "description": ""
        },
        {
            "id": "MIM:300067",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300067",
            "name": "Subcortical band heterotopia X-linked",
            "description": "Subcortical band heterotopia X-linked"
        }
    ]
}