{
    "disease_id": "DOID:0110241",
    "recommended_name": {
        "id": "DOID:0110241",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110241",
        "name": "cataract 41",
        "description": "A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16."
    },
    "synonyms": [
        {
            "id": "DOID:0110241",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110241",
            "name": "CTRCT41",
            "description": ""
        },
        {
            "id": "DOID:0110241",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110241",
            "name": "congenital nuclear type cataract 41",
            "description": ""
        },
        {
            "id": "MONDO:0007287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007287",
            "name": "cataract 41",
            "description": "Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the WFS1 gene."
        },
        {
            "id": "MONDO:0007287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007287",
            "name": "cataract 41; CTRCT41",
            "description": ""
        },
        {
            "id": "MONDO:0007287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007287",
            "name": "congenital nuclear type cataract 41",
            "description": ""
        },
        {
            "id": "MONDO:0007287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007287",
            "name": "cataract 41",
            "description": ""
        },
        {
            "id": "MONDO:0007287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007287",
            "name": "CTRCT41",
            "description": ""
        },
        {
            "id": "MONDO:0007287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007287",
            "name": "WFS1 early-onset non-syndromic cataract",
            "description": ""
        },
        {
            "id": "MONDO:0007287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007287",
            "name": "early-onset non-syndromic cataract caused by mutation in WFS1",
            "description": ""
        },
        {
            "id": "MONDO:0007287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007287",
            "name": "cataract 41, congenital nuclear type",
            "description": ""
        },
        {
            "id": "MONDO:0007287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007287",
            "name": "cataract type 41",
            "description": ""
        },
        {
            "id": "MIM:116400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/116400",
            "name": "Cataract 41",
            "description": "Cataract 41"
        }
    ]
}