{
    "disease_id": "DOID:0110263", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014111", 
            "name": "cataract type 19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014111", 
            "name": "LIM2 early-onset non-syndromic cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014111", 
            "name": "CTRCT19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014111", 
            "name": "cataract 19, multiple types; CTRCT19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014111", 
            "name": "cataract 19, multiple types"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014111", 
            "name": "early-onset non-syndromic cataract caused by mutation in LIM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014111", 
            "name": "cataract 19; CTRCT19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014111", 
            "name": "cataract 19"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110263", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110263", 
            "name": "CTRCT19"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110263", 
        "description": "A cataract that has_material_basis_in homozygous mutation in the LIM2 gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110263", 
        "name": "cataract 19 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110263#disease-associations", 
            "id": "0110263", 
            "database": "Alliance of Genome Resources"
        }
    ]
}