{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012456", 
            "name": "congenital primary aphakia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012456", 
            "name": "congenital aphakia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012456", 
            "name": "CPA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012456", 
            "name": "aphakia, congenital primary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012456", 
            "name": "ASGD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012456", 
            "name": "congenital absence of lens"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012456", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012456", 
            "name": "anterior segment dysgenesis 2; ASGD2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080607", 
        "description": "An anterior segment dysgenesis that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the FOXE3 gene on chromosome 1p33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080607", 
        "name": "anterior segment dysgenesis 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610256", 
            "id": "610256", 
            "database": "MIM"
        }
    ]
}