{
    "disease_id": "DOID:0110245", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013859", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013859", 
            "name": "CATC5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013859", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013859", 
            "name": "AGK early-onset non-syndromic cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013859", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013859", 
            "name": "cataract, autosomal recessive congenital 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013859", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013859", 
            "name": "cataract 38; CTRCT38"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013859", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013859", 
            "name": "CTRCT38"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013859", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013859", 
            "name": "early-onset non-syndromic cataract caused by mutation in AGK"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013859", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013859", 
            "name": "autosomal recessive congenital cataract 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013859", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013859", 
            "name": "cataract type 38"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110245", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110245", 
            "name": "CATC5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110245", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110245", 
            "name": "CTRCT38"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110245", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110245", 
            "name": "autosomal recessive congenital cataract 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110245", 
        "description": "A cataract that has_material_basis_in homozygous mutation in the AGK gene on chromosome 7q34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110245", 
        "name": "cataract 38"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614691", 
            "id": "614691", 
            "database": "MIM"
        }
    ]
}