{
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    "synonyms": [
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            "description": "", 
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            "description": "", 
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        {
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008799", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008799", 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008799", 
            "name": "optic nerve hypoplasia and abnormalities of the central nervous system"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111801", 
            "name": "AEG syndrome"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "MCOPS3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111801", 
            "name": "SOX2 anophthalmia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111801", 
            "name": "anophthalmia clinical with associated anomalies"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111801", 
            "name": "anophthalmia esophageal genital syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111801", 
            "name": "anophthalmia microphthalmia esophageal atresia"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "microphthalmia and esophageal atresia syndrome"
        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
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            "description": "", 
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            "id": "DOID:0111801", 
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111801", 
        "description": "A syndromic microphthalmia characterized by clinical anophthalmia or microphthalmia, with various extraocular symptoms that has_material_basis_in heterozygous mutation in SOX2 on chromosome 3q26.33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111801", 
        "name": "syndromic microphthalmia 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111801#disease-associations", 
            "id": "0111801", 
            "database": "Alliance of Genome Resources"
        }
    ]
}