{
    "disease_id": "DOID:0110268", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012336", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012336", 
            "name": "CTRCT22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012336", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012336", 
            "name": "early-onset non-syndromic cataract caused by mutation in CRYBB3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012336", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012336", 
            "name": "cataract 22, multiple types"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012336", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012336", 
            "name": "cataract 22, multiple types; CTRCT22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012336", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012336", 
            "name": "autosomal recessive congenital nuclear cataract 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012336", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012336", 
            "name": "CATCN2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012336", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012336", 
            "name": "CRYBB3 early-onset non-syndromic cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012336", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012336", 
            "name": "cataract, congenital nuclear, autosomal recessive 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110268", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110268", 
            "name": "CTRCT22"
        }, 
        {
            "url": "https://www.omim.org/entry/609741", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:609741", 
            "name": "Cataract 22, multiple types"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110268", 
        "description": "A cataract that has_material_basis_in heterozygous or homozygous mutation in the beta-B3 crystallin gene (CRYBB3) on chromosome 22q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110268", 
        "name": "cataract 22 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/609741", 
            "id": "609741", 
            "database": "MIM"
        }
    ]
}