{
    "disease_id": "DOID:0110236", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014075", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014075", 
            "name": "CTRCT39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014075", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014075", 
            "name": "cataract 39, multiple types"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014075", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014075", 
            "name": "early-onset non-syndromic cataract caused by mutation in CRYGB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014075", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014075", 
            "name": "autosomal dominant cataract 39 multiple types"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014075", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014075", 
            "name": "CRYGB early-onset non-syndromic cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014075", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014075", 
            "name": "cataract 39, multiple types; CTRCT39"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110236", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110236", 
            "name": "CTRCT39"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110236", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110236", 
            "name": "autosomal dominant cataract 39 multiple types"
        }, 
        {
            "url": "https://www.omim.org/entry/615188", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615188", 
            "name": "Cataract 39, multiple types"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110236", 
        "description": "A cataract  that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110236", 
        "name": "cataract 39 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615188", 
            "id": "615188", 
            "database": "MIM"
        }
    ]
}