{
    "disease_id": "DOID:0060902", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009760", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009760", 
            "name": "Microlissencephaly type A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009760", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009760", 
            "name": "LIS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009760", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009760", 
            "name": "lissencephaly type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009760", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009760", 
            "name": "lissencephaly syndrome Norman-Roberts type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009760", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009760", 
            "name": "lissencephaly syndrome, Norman-Roberts type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009760", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009760", 
            "name": "lissencephaly 2; LIS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009760", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009760", 
            "name": "lissencephaly 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009760", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009760", 
            "name": "Norman Roberts lissencephaly syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060902", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060902", 
            "name": "lissencephaly 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060902", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060902", 
            "name": "lissencephaly syndrome, Norman-Roberts type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060902", 
        "description": "A lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060902", 
        "name": "Norman-Roberts syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060902#disease-associations", 
            "id": "0060902", 
            "database": "Alliance of Genome Resources"
        }
    ]
}