{
    "disease_id": "DOID:0060305",
    "recommended_name": {
        "id": "DOID:0060305",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060305",
        "name": "megalocornea",
        "description": "A corneal disease that is characterized by a bilaterally enlarged corneal diameter without an increase in intraocular pressure and that has_material_basis_in mutation in the CHRDL1 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0060305",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060305",
            "name": "anterior megalophthalmos",
            "description": ""
        },
        {
            "id": "DOID:0060305",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060305",
            "name": "congenital anterior megalophthalmia",
            "description": ""
        },
        {
            "id": "MONDO:0009576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009576",
            "name": "megalocornea (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0009576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009576",
            "name": "congenital anterior megalophthalmia",
            "description": ""
        },
        {
            "id": "MONDO:0009576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009576",
            "name": "anterior megalophthalmos",
            "description": ""
        },
        {
            "id": "MONDO:0009576",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009576",
            "name": "megalocornea",
            "description": ""
        },
        {
            "id": "MONDO:0010649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010649",
            "name": "isolated congenital megalocornea",
            "description": "12.5 mm) and a deep anterior eye chamber, without an elevation in intraocular pressure. It can manifest with mild to moderate myopia as well as photophobia and iridodonesis (due to iris hypoplasia). Associated complications include lens dislocation, retinal detachment, presenile cataract development, and secondary glaucoma."
        },
        {
            "id": "MONDO:0010649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010649",
            "name": "MGC1",
            "description": ""
        },
        {
            "id": "MONDO:0010649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010649",
            "name": "congenital anterior megalophthalmia",
            "description": ""
        },
        {
            "id": "MONDO:0010649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010649",
            "name": "megalocornea; MGC1",
            "description": ""
        },
        {
            "id": "MONDO:0010649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010649",
            "name": "Mgcn",
            "description": ""
        },
        {
            "id": "MONDO:0010649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010649",
            "name": "megalocornea",
            "description": ""
        },
        {
            "id": "MIM:309300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/309300",
            "name": "Megalocornea 1, X-linked",
            "description": "Megalocornea 1, X-linked"
        }
    ]
}