{
    "disease_id": "DOID:0060838", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013377", 
            "name": "microphthalmia, isolated 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013377", 
            "name": "GDF3 isolated microphthalmia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013377", 
            "name": "microphthalmia, isolated type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013377", 
            "name": "isolated microphthalmia caused by mutation in GDF3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013377", 
            "name": "MCOP7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013377", 
            "name": "isolated microphthalmia type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013377", 
            "name": "microphthalmia, isolated 7; MCOP7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060838", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060838", 
            "name": "MCOP7"
        }, 
        {
            "url": "https://www.omim.org/entry/613704", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613704", 
            "name": "Microphthalmia, isolated, 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060838", 
        "description": "An isolated microphthalmia characterized by unilateral microphthalmia that has_material_basis_in caused by mutation in the GDF3 gene on chromosome 12p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060838", 
        "name": "isolated microphthalmia 7"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613704", 
            "id": "613704", 
            "database": "MIM"
        }
    ]
}