{
    "disease_id": "DOID:0110269", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011104", 
            "name": "cataract 3, multiple types, with or without microcornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011104", 
            "name": "CTRCT3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011104", 
            "name": "congenital cerulean type cataract 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011104", 
            "name": "cataract (disease) caused by mutation in CRYBB2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011104", 
            "name": "cataract 3, multiple types"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011104", 
            "name": "cataract, congenital, cerulean type, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011104", 
            "name": "CRYBB2 cataract (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011104", 
            "name": "cataract 3 multiple types with or without microcornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011104", 
            "name": "CCA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011104", 
            "name": "cataract 3, multiple types; CTRCT3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110269", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110269", 
            "name": "CTRCT3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110269", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110269", 
            "name": "cataract 3 multiple types with or without microcornea"
        }, 
        {
            "url": "https://www.omim.org/entry/601547", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:601547", 
            "name": "Cataract 3, multiple types"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110269", 
        "description": "A cataract that has_material_basis_in heterozygous mutation in the beta-B2-crystallin gene (CRYBB2) on chromosome 22q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110269", 
        "name": "cataract 3 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/601547", 
            "id": "601547", 
            "database": "MIM"
        }
    ]
}