{
    "disease_id": "DOID:0111804", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013734", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013734", 
            "name": "microphthalmia, syndromic 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013734", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013734", 
            "name": "microphthalmia, syndromic type 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013734", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013734", 
            "name": "VAX1 syndromic microphthalmia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013734", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013734", 
            "name": "syndromic microphthalmia caused by mutation in VAX1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013734", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013734", 
            "name": "microphthalmia, syndromic 11; MCOPS11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013734", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013734", 
            "name": "MCOPS11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111804", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111804", 
            "name": "MCOPS11"
        }, 
        {
            "url": "https://www.omim.org/entry/614402", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614402", 
            "name": "Microphthalmia, syndromic, 11"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111804", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111804", 
        "name": "syndromic microphthalmia 11"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614402", 
            "id": "614402", 
            "database": "MIM"
        }
    ]
}