{
    "disease_id": "DOID:0080610", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011414", 
            "name": "Peters anomaly (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011414", 
            "name": "Peters anomaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011414", 
            "name": "ASGD5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011414", 
            "name": "anterior segment dysgenesis 5; ASGD5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011414", 
            "name": "Peters congenital glaucoma"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080610", 
        "description": "An anterior segment dysgenesis that has_material_basis_in heterozygous mutation in the PAX6 gene on chromosome 11p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080610", 
        "name": "anterior segment dysgenesis 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/604229", 
            "id": "604229", 
            "database": "MIM"
        }
    ]
}