{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "cataract, age-related cortical, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "cataract 6, multiple types"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "cataract 6, multiple types; CTRCT6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "CTPA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "CTPP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "Posterior polar cataract, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "age related cortical cataract 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "cataract (disease) caused by mutation in EPHA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "cataract, posterior polar, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "ARCC2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "EPHA2 cataract (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "CTPP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "posterior polar cataract 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007288", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007288", 
            "name": "CTRCT6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110229", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110229", 
            "name": "CTRCT6"
        }, 
        {
            "url": "https://www.omim.org/entry/116600", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:116600", 
            "name": "Cataract 6, multiple types"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110229", 
        "description": "A cataract that has_material_basis_in heterozygous mutation in the EPHA2 gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110229", 
        "name": "cataract 6 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/116600", 
            "id": "116600", 
            "database": "MIM"
        }
    ]
}