{
    "disease_id": "DOID:0050453", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014077", 
            "name": "cobblestone lissencephaly without muscular or ocular involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014077", 
            "name": "lissencephaly 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014077", 
            "name": "lissencephaly type 2 without muscular or eye involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014077", 
            "name": "cobblestone lissencephaly without muscular or eye involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014077", 
            "name": "LIS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014077", 
            "name": "lissencephaly type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014077", 
            "name": "lissencephaly type 2 without muscular or ocular involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014077", 
            "name": "lissencephaly 5; LIS5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050453", 
        "description": "A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050453", 
        "name": "lissencephaly"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050453#disease-associations", 
            "id": "0050453", 
            "database": "Alliance of Genome Resources"
        }
    ]
}