{
    "disease_id": "DOID:0110234", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "CCA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "CRYGD cataract (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "cataract, congenital, cerulean type, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "cataract 4 multiple types with or without microcornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "cataract 4, multiple types"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "cataract, Nonnuclear polymorphic congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "cataract, crystalline aculeiform"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "cataract, punctate, progressive juvenile-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "cataract 4, multiple types; CTRCT4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "CTRCT4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "congenital cataract cerulean type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "cataract 4, multiple types, with or without microcornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007281", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007281", 
            "name": "cataract (disease) caused by mutation in CRYGD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110234", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110234", 
            "name": "CTRCT4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110234", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110234", 
            "name": "cataract 4 multiple types with or without microcornea"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110234", 
        "description": "A cataract that has_material_basis_in heterozygous mutation in the gamma-D-crystallin gene (CRYGD) on chromosome 2q33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110234", 
        "name": "cataract 4 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110234#disease-associations", 
            "id": "0110234", 
            "database": "Alliance of Genome Resources"
        }
    ]
}