{
    "disease_id": "DOID:0110241", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007287", 
            "name": "cataract 41; CTRCT41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007287", 
            "name": "congenital nuclear type cataract 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007287", 
            "name": "CTRCT41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007287", 
            "name": "WFS1 early-onset non-syndromic cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007287", 
            "name": "early-onset non-syndromic cataract caused by mutation in WFS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007287", 
            "name": "cataract 41, congenital nuclear type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007287", 
            "name": "cataract type 41"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110241", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110241", 
            "name": "CTRCT41"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110241", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110241", 
            "name": "congenital nuclear type cataract 41"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110241", 
        "description": "A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110241", 
        "name": "cataract 41"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110241#disease-associations", 
            "id": "0110241", 
            "database": "Alliance of Genome Resources"
        }
    ]
}