{
    "disease_id": "DOID:0111648",
    "recommended_name": {
        "id": "DOID:0111648",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111648",
        "name": "ectopia lentis with ectopia of pupil",
        "description": "An eye disease characterized by displacement of the lenses and the pupils in association with other ocular anomalies that has_material_basis_in homozygous or compound heterozygous mutation mutation in the ADAMTSL4 gene on chromosome 1q21.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111648",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111648",
            "name": "ectopia lentis et pupillae",
            "description": ""
        },
        {
            "id": "MONDO:0009153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009153",
            "name": "ectopia lentis et pupillae",
            "description": ""
        },
        {
            "id": "MONDO:0009153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009153",
            "name": "ectopia lentis et pupillae",
            "description": ""
        },
        {
            "id": "MIM:225200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/225200",
            "name": "Ectopia lentis et pupillae",
            "description": "Ectopia lentis et pupillae"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111648"
    ],
    "unlinked_id_list": []
}