{
    "disease_id": "DOID:0060852", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012184", 
            "name": "microcoria-congenital nephrosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012184", 
            "name": "microcoria-congenital nephrotic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012184", 
            "name": "microcoria - congenital nephrotic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012184", 
            "name": "microcoria - congenital nephrosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060852", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060852", 
            "name": "microcoria-congenital nephrosis syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060852", 
        "description": "A syndrome characterized by nephrotic syndrome with diffuse mesangial sclerosis, proteinuria, microcoria, absence of the pupillary dilator muscle in the iris, ciliary muscle atrophy, and abnormal eye development with lens-shape, retinal and corneal anomalies that has_material_basis_in homozygous or compound heterozygous mutation in the LAMB2 on chromosome 3p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060852", 
        "name": "Pierson syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060852#disease-associations", 
            "id": "0060852", 
            "database": "Alliance of Genome Resources"
        }
    ]
}