{
    "disease_id": "DOID:0080669", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054832", 
            "name": "corneal dystrophy, posterior polymorphous, 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054832", 
            "name": "corneal dystrophy, POSTERIOR polymorphous, 4; PPCD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054832", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054832", 
            "name": "PPCD4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080669", 
        "description": "A posterior polymorphous corneal dystrophy that is characterized by an irregular posterior corneal surface with occasional opacities of variable size and shape and that has_material_basis_in heterozygous mutation in the GRHL2 gene on chromosome 8q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080669", 
        "name": "posterior polymorphous corneal dystrophy 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080669#disease-associations", 
            "id": "0080669", 
            "database": "Alliance of Genome Resources"
        }
    ]
}