{
    "disease_id": "DOID:0111804",
    "recommended_name": {
        "id": "DOID:0111804",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111804",
        "name": "syndromic microphthalmia 11",
        "description": "A syndromic microphthalmia characterized by  microphthalmia, cleft lip and palate, and agenesis of the corpus callosum that has_material_basis_in homozygous or compound heterozygous mutation in VAX1 on chromosome 10q25.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111804",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111804",
            "name": "MCOPS11",
            "description": ""
        },
        {
            "id": "MONDO:0013734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013734",
            "name": "microphthalmia, syndromic 11",
            "description": "Any syndromic microphthalmia in which the cause of the disease is a mutation in the VAX1 gene."
        },
        {
            "id": "MONDO:0013734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013734",
            "name": "microphthalmia, syndromic type 11",
            "description": ""
        },
        {
            "id": "MONDO:0013734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013734",
            "name": "microphthalmia, syndromic 11",
            "description": ""
        },
        {
            "id": "MONDO:0013734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013734",
            "name": "VAX1 syndromic microphthalmia",
            "description": ""
        },
        {
            "id": "MONDO:0013734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013734",
            "name": "syndromic microphthalmia caused by mutation in VAX1",
            "description": ""
        },
        {
            "id": "MONDO:0013734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013734",
            "name": "microphthalmia, syndromic 11; MCOPS11",
            "description": ""
        },
        {
            "id": "MONDO:0013734",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013734",
            "name": "MCOPS11",
            "description": ""
        },
        {
            "id": "MIM:614402",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614402",
            "name": "Microphthalmia, syndromic, 11",
            "description": "Microphthalmia, syndromic, 11"
        }
    ]
}