{
    "disease_id": "DOID:0080530", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "granular corneal dystrophy type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "granular corneal dystrophy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "corneal dystrophy Groenouw type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "classic granular corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "Groenouw type I corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "corneal dystrophy, Groenouw type I; CDGG1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "granular corneal dystrophy, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "GCDI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "corneal dystrophy granular type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "corneal dystrophy, Groenouw type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "corneal dystrophy punctate or nodular"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "corneal dystrophy, Groenouw type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "classic GCD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "GCD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "corneal dystrophy, punctate or nodular"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007377", 
            "name": "CDGG1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080530", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080530", 
            "name": "corneal dystrophy, Groenouw type I"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080530", 
        "description": "A granular corneal dystrophy that is characterized by recurrent erosions and gray crumb-like opacification located_in the cornea, proteinaceous rock candy-like deposits in the anterior stroma and subepithelium, and progressive vision loss later in life as deposits move into the central vision, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased protein deposition and disruption of the corneal surface.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080530", 
        "name": "granular corneal dystrophy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080530#disease-associations", 
            "id": "0080530", 
            "database": "Alliance of Genome Resources"
        }
    ]
}