{
    "disease_id": "DOID:0110265", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011547", 
            "name": "cataract, posterior polar, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011547", 
            "name": "CTRCT31"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011547", 
            "name": "CTPP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011547", 
            "name": "posterior polar cataract 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011547", 
            "name": "early-onset non-syndromic cataract caused by mutation in CHMP4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011547", 
            "name": "CPP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011547", 
            "name": "CHMP4B early-onset non-syndromic cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011547", 
            "name": "cataract 31, multiple types; CTRCT31"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011547", 
            "name": "cataract 31, multiple types"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110265", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110265", 
            "name": "CTRCT31"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110265", 
        "description": "A cataract that has_material_basis_in heterozygous mutation in the CHMP4B gene on chromosome 20q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110265", 
        "name": "cataract 31 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110265#disease-associations", 
            "id": "0110265", 
            "database": "Alliance of Genome Resources"
        }
    ]
}