{
    "disease_id": "DOID:0110266",
    "recommended_name": {
        "id": "DOID:0110266",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110266",
        "name": "cataract 9 multiple types",
        "description": "A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110266",
            "name": "cataract 9 multiple types with or without microcornea",
            "description": ""
        },
        {
            "id": "DOID:0110266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110266",
            "name": "CTRCT9",
            "description": ""
        },
        {
            "id": "MONDO:0011413",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011413",
            "name": "cataract 9 multiple types",
            "description": "Any cataract (disease) in which the cause of the disease is a mutation in the CRYAA gene."
        },
        {
            "id": "MONDO:0011413",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011413",
            "name": "CRYAA cataract (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0011413",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011413",
            "name": "CTRCT9",
            "description": ""
        },
        {
            "id": "MONDO:0011413",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011413",
            "name": "cataract (disease) caused by mutation in CRYAA",
            "description": ""
        },
        {
            "id": "MONDO:0011413",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011413",
            "name": "cataract 9, multiple types",
            "description": ""
        },
        {
            "id": "MIM:604219",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604219",
            "name": "Cataract 9, multiple types",
            "description": "Cataract 9, multiple types"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110266"
    ],
    "unlinked_id_list": []
}