{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013293", 
            "name": "microphthalmia, isolated type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013293", 
            "name": "microphthalmia, posterior nonsyndromic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013293", 
            "name": "MCOP6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013293", 
            "name": "PRSS56 isolated microphthalmia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013293", 
            "name": "microphthalmia, isolated 6; MCOP6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013293", 
            "name": "posterior nonsyndromic microphthalmia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013293", 
            "name": "isolated microphthalmia type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013293", 
            "name": "isolated microphthalmia caused by mutation in PRSS56"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013293", 
            "name": "microphthalmia, isolated 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060835", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060835", 
            "name": "MCOP6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060835", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060835", 
            "name": "posterior nonsyndromic microphthalmia"
        }, 
        {
            "url": "https://www.omim.org/entry/613517", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613517", 
            "name": "Microphthalmia, isolated, 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060835", 
        "description": "An isolated microphthalmia characterized by autosomal recessive inheritance reduction in eye size that is restricted to the posterior segment of the eye, extreme hyperopia, and short axial length that has_material_basis_in homozygous or compound heterozygous mutation in the PRSS56 gene on chromosome 2q37.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060835", 
        "name": "isolated microphthalmia 6"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613517", 
            "id": "613517", 
            "database": "MIM"
        }
    ]
}