{
    "disease_id": "DOID:0110238", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012395", 
            "name": "FYCO1 cataract (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012395", 
            "name": "cataract type 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012395", 
            "name": "cataract 18 autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012395", 
            "name": "cataract (disease) caused by mutation in FYCO1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012395", 
            "name": "cataract 18; CTRCT18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012395", 
            "name": "autosomal recessive congenital cataract 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012395", 
            "name": "cataract, autosomal recessive congenital 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012395", 
            "name": "CTRCT18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012395", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012395", 
            "name": "CATC2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110238", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110238", 
            "name": "CATC2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110238", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110238", 
            "name": "CTRCT18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110238", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110238", 
            "name": "autosomal recessive congenital cataract 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110238", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110238", 
            "name": "cataract 18 autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110238", 
        "description": "A cataract that has_material_basis_in homozygous mutation in the FYCO1 gene on chromosome 3p21.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110238", 
        "name": "cataract 18"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110238#disease-associations", 
            "id": "0110238", 
            "database": "Alliance of Genome Resources"
        }
    ]
}