{
    "disease_id": "DOID:0110243",
    "recommended_name": {
        "id": "DOID:0110243",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110243",
        "name": "cataract 46 juvenile-onset",
        "description": "A cataract that has_material_basis_in homozygous mutation in the LEMD2 gene on chromosome 6p21."
    },
    "synonyms": [
        {
            "id": "DOID:0110243",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110243",
            "name": "CTRCT46",
            "description": ""
        },
        {
            "id": "DOID:0110243",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110243",
            "name": "juvenilae cataract Hutterite type",
            "description": ""
        },
        {
            "id": "MONDO:0008925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008925",
            "name": "cataract 46 juvenile-onset",
            "description": "Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the LEMD2 gene."
        },
        {
            "id": "MONDO:0008925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008925",
            "name": "CTRCT46",
            "description": ""
        },
        {
            "id": "MONDO:0008925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008925",
            "name": "LEMD2 early-onset non-syndromic cataract",
            "description": ""
        },
        {
            "id": "MONDO:0008925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008925",
            "name": "early-onset non-syndromic cataract caused by mutation in LEMD2",
            "description": ""
        },
        {
            "id": "MONDO:0008925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008925",
            "name": "juvenilae cataract Hutterite type",
            "description": ""
        },
        {
            "id": "MONDO:0008925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008925",
            "name": "cataract 46, juvenile-onset",
            "description": ""
        },
        {
            "id": "MONDO:0008925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008925",
            "name": "cataract Hutterite type",
            "description": ""
        },
        {
            "id": "MONDO:0008925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008925",
            "name": "cataract, congenital or juvenile",
            "description": ""
        },
        {
            "id": "MONDO:0008925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008925",
            "name": "cataract, juvenile, Hutterite type",
            "description": ""
        },
        {
            "id": "MIM:212500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/212500",
            "name": "Cataract 46, juvenile-onset, with or without arrhythmic cardiomyopathy",
            "description": "Cataract 46, juvenile-onset, with or without arrhythmic cardiomyopathy"
        }
    ]
}