{
    "disease_id": "DOID:0110243", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008925", 
            "name": "cataract 46, juvenile-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008925", 
            "name": "cataract, congenital or juvenile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008925", 
            "name": "LEMD2 early-onset non-syndromic cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008925", 
            "name": "cataract Hutterite type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008925", 
            "name": "juvenilae cataract Hutterite type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008925", 
            "name": "cataract, juvenile, Hutterite type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008925", 
            "name": "early-onset non-syndromic cataract caused by mutation in LEMD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008925", 
            "name": "CTRCT46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008925", 
            "name": "cataract 46, juvenile-onset; CTRCT46"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110243", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110243", 
            "name": "CTRCT46"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110243", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110243", 
            "name": "juvenilae cataract Hutterite type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110243", 
        "description": "A cataract that has_material_basis_in homozygous mutation in the LEMD2 gene on chromosome 6p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110243", 
        "name": "cataract 46 juvenile-onset"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110243#disease-associations", 
            "id": "0110243", 
            "database": "Alliance of Genome Resources"
        }
    ]
}