{
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            "description": "", 
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            "description": "", 
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        }, 
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "cataract 34, multiple types; CTRCT34"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013067", 
            "name": "cataract 34, multiple types, with or without microcornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013067", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "cataract 34 multiple types with or without microcornea"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013067", 
            "name": "cataract, autosomal recessive congenital 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013067", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013067", 
            "name": "cataract (disease) caused by mutation in FOXE3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013067", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013067", 
            "name": "CTRCT34"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013067", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013067", 
            "name": "FOXE3 cataract (disease)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110230", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110230", 
            "name": "CATC3"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110230", 
            "name": "CTRCT34"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110230", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110230", 
            "name": "autosomal recessive congenital cataract 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110230", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110230", 
            "name": "cataract 34 multiple types with or without microcornea"
        }, 
        {
            "url": "https://www.omim.org/entry/612968", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:612968", 
            "name": "Cataract 34, multiple types"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110230", 
        "description": "A cataract that has_material_basis_in variation in the region 1p34.3-p32.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110230", 
        "name": "cataract 34 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612968", 
            "id": "612968", 
            "database": "MIM"
        }
    ]
}
