{
    "disease_id": "DOID:0110856", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012199", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012199", 
            "name": "COL8A2 posterior polymorphous corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012199", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012199", 
            "name": "corneal dystrophy, posterior polymorphous, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012199", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012199", 
            "name": "posterior polymorphous corneal dystrophy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012199", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012199", 
            "name": "posterior polymorphous corneal dystrophy caused by mutation in COL8A2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012199", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012199", 
            "name": "corneal dystrophy, POSTERIOR polymorphous, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012199", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012199", 
            "name": "PPCD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012199", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012199", 
            "name": "corneal dystrophy, POSTERIOR polymorphous, 2; PPCD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110856", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110856", 
            "name": "Ppcd2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110856", 
        "description": "A posterior polymorphous corneal dystrophy that has_material_basis_in heterozygous mutation in the COL8A2 gene on chromosome 1p34.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110856", 
        "name": "posterior polymorphous corneal dystrophy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110856#disease-associations", 
            "id": "0110856", 
            "database": "Alliance of Genome Resources"
        }
    ]
}