{
    "disease_id": "DOID:0110855", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "corneal dystrophy, hereditary polymorphous posterior"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "corneal dystrophy, POSTERIOR polymorphous, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "corneal dystrophy, POSTERIOR polymorphous, 1; PPCD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "PPCD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "posterior polymorphous corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "corneal endothelial dystrophy 1, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "corneal endothelial dystrophy 1, autosomal dominant, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "Ched1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "Maumenee corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "corneal dystrophy, posterior polymorphous, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007378", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007378", 
            "name": "posterior polymorphous corneal dystrophy type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110855", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110855", 
            "name": "Corneal Endothelial Dystrophy 1, Autosomal Dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110855", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110855", 
            "name": "Ched1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110855", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110855", 
            "name": "Maumenee Corneal Dystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110855", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110855", 
            "name": "Ppcd1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110855", 
        "description": "A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110855", 
        "name": "posterior polymorphous corneal dystrophy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110855#disease-associations", 
            "id": "0110855", 
            "database": "Alliance of Genome Resources"
        }
    ]
}