{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012604", 
            "name": "isolated microphthalmia caused by mutation in RAX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012604", 
            "name": "RAX isolated microphthalmia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012604", 
            "name": "microphthalmia, isolated 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012604", 
            "name": "MCOP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012604", 
            "name": "isolated microphthalmia type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012604", 
            "name": "microphthalmia, isolated type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012604", 
            "name": "microphthalmia, isolated 3; MCOP3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060842", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060842", 
            "name": "MCOP3"
        }, 
        {
            "url": "https://www.omim.org/entry/611038", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:611038", 
            "name": "Microphthalmia, isolated, 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060842", 
        "description": "An isolated microphthalmia characterized by clinical anophthalmia and/or microphthalmia that has_material_basis_in compound heterozygous mutation in the RAX gene on chromosome 18q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060842", 
        "name": "isolated microphthalmia 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/611038", 
            "id": "611038", 
            "database": "MIM"
        }
    ]
}