{
    "disease_id": "DOID:0112231",
    "recommended_name": {
        "id": "DOID:0112231",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112231",
        "name": "lissencephaly 7 with cerebellar hypoplasia",
        "description": "A lissencephaly characterized by lack of psychomotor development, facial dysmorphism, arthrogryposis, and early-onset intractable seizures resulting in death in infancy that has_material_basis_in homozygous or compound heterozygous mutation in the CDK5 gene on chromosome 7q36.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112231",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112231",
            "name": "LIS7",
            "description": ""
        },
        {
            "id": "MONDO:0014596",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014596",
            "name": "lissencephaly 7 with cerebellar hypoplasia",
            "description": ""
        },
        {
            "id": "MONDO:0014596",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014596",
            "name": "lissencephaly 7 with cerebellar hypoplasia",
            "description": ""
        },
        {
            "id": "MONDO:0014596",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014596",
            "name": "LIS7",
            "description": ""
        },
        {
            "id": "MIM:616342",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616342",
            "name": "Lissencephaly 7, with cerebellar hypoplasia",
            "description": "Lissencephaly 7, with cerebellar hypoplasia"
        }
    ]
}