{
    "disease_id": "DOID:0070532",
    "recommended_name": {
        "id": "DOID:0070532",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070532",
        "name": "aniridia 1",
        "description": "An aniridia that has_material_basis_in heterozygous mutation in the PAX6 gene on chromosome 11p13. Additional ocular anomalies are also common."
    },
    "synonyms": [
        {
            "id": "MONDO:0024507",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024507",
            "name": "aniridia 1",
            "description": ""
        },
        {
            "id": "MONDO:0024507",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024507",
            "name": "aniridia",
            "description": ""
        },
        {
            "id": "MONDO:0024507",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024507",
            "name": "AN1",
            "description": ""
        },
        {
            "id": "MONDO:0024507",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024507",
            "name": "aniridia 1",
            "description": ""
        },
        {
            "id": "MONDO:0024507",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024507",
            "name": "cataract with late-onset corneal dystrophy",
            "description": ""
        },
        {
            "id": "MIM:106210",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/106210",
            "name": "Aniridia 1",
            "description": "Aniridia 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070532"
    ],
    "unlinked_id_list": []
}