{
    "disease_id": "DOID:0060902",
    "recommended_name": {
        "id": "DOID:0060902",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060902",
        "name": "Norman-Roberts syndrome",
        "description": "A lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22."
    },
    "synonyms": [
        {
            "id": "DOID:0060902",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060902",
            "name": "lissencephaly 2",
            "description": ""
        },
        {
            "id": "DOID:0060902",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060902",
            "name": "lissencephaly syndrome, Norman-Roberts type",
            "description": ""
        },
        {
            "id": "MONDO:0009760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009760",
            "name": "Norman-Roberts syndrome",
            "description": "Lissencephaly syndrome, Norman-Roberts type is characterized by the association of lissencephaly type I with craniofacial anomalies (severe microcephaly, a low sloping forehead, a broad and prominent nasal bridge and widely set eyes) and postnatal growth retardation."
        },
        {
            "id": "MONDO:0009760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009760",
            "name": "Microlissencephaly type A",
            "description": ""
        },
        {
            "id": "MONDO:0009760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009760",
            "name": "Norman-Roberts syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009760",
            "name": "lissencephaly 2",
            "description": ""
        },
        {
            "id": "MONDO:0009760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009760",
            "name": "lissencephaly 2 (Norman-Roberts type)",
            "description": ""
        },
        {
            "id": "MONDO:0009760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009760",
            "name": "lissencephaly syndrome, Norman-Roberts type",
            "description": ""
        },
        {
            "id": "MONDO:0009760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009760",
            "name": "LIS2",
            "description": ""
        },
        {
            "id": "MONDO:0009760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009760",
            "name": "Norman Roberts lissencephaly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009760",
            "name": "lissencephaly syndrome Norman-Roberts type",
            "description": ""
        },
        {
            "id": "MIM:257320",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/257320",
            "name": "Lissencephaly 2",
            "description": "Lissencephaly 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060902"
    ],
    "unlinked_id_list": []
}