{
    "disease_id": "DOID:0050593",
    "recommended_name": {
        "id": "DOID:0050593",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050593",
        "name": "primary congenital glaucoma",
        "description": "A glaucoma that is characterized by damage to the optic nerves that reduces peripheral vision and leads to blindness, has_material_basis_in mutation in the MYOC gene and appears before the age of 5 without other associated abnormalities."
    },
    "synonyms": [
        {
            "id": "MONDO:0013121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013121",
            "name": "glaucoma 3, primary congenital, C",
            "description": ""
        },
        {
            "id": "MONDO:0013121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013121",
            "name": "GLC3C",
            "description": ""
        },
        {
            "id": "MONDO:0013121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013121",
            "name": "glaucoma 3, primary congenital, C",
            "description": ""
        },
        {
            "id": "MONDO:0013122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013122",
            "name": "glaucoma 3, primary congenital, D",
            "description": ""
        },
        {
            "id": "MONDO:0013122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013122",
            "name": "glaucoma 3, primary congenital, D",
            "description": ""
        },
        {
            "id": "MONDO:0013122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013122",
            "name": "glaucoma 3, primary congenital, type D",
            "description": ""
        },
        {
            "id": "MONDO:0013122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013122",
            "name": "GLC3D",
            "description": ""
        },
        {
            "id": "MIM:613086",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613086",
            "name": "Glaucoma 3, primary congenital, D",
            "description": "Glaucoma 3, primary congenital, D"
        }
    ],
    "children": [
        {
            "id": "DOID:11212",
            "label": "hydrophthalmos",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:11211",
                    "label": "buphthalmos",
                    "link_status": true,
                    "children": []
                }
            ]
        }
    ],
    "id_list": [
        "DOID:0050593",
        "DOID:11212",
        "DOID:11211"
    ],
    "unlinked_id_list": []
}