{
    "disease_id": "DOID:0110256", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "congenital cataract cerulean type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "cataract 21, multiple types; CTRCT21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "cataract 21, multiple types"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "MAF early-onset non-syndromic cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "cataract, congenital, cerulean type, 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "early-onset non-syndromic cataract caused by mutation in MAF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "cataract 21, multiple types, with or without microcornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "CCA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "cataract, pulverulent, juvenile-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "CTRCT21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012437", 
            "name": "cataract 21 multiple types with or without microcornea"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110256", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110256", 
            "name": "CTRCT21"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110256", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110256", 
            "name": "cataract 21 multiple types with or without microcornea"
        }, 
        {
            "url": "https://www.omim.org/entry/610202", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:610202", 
            "name": "Cataract 21, multiple types"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110256", 
        "description": "A cataract that has_material_basis_in heterozygous mutation in the MAF gene on chromosome 16q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110256", 
        "name": "cataract 21 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610202", 
            "id": "610202", 
            "database": "MIM"
        }
    ]
}