{
    "disease_id": "DOID:0060444",
    "recommended_name": {
        "id": "DOID:0060444",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060444",
        "name": "granular corneal dystrophy 2",
        "description": "An corneal granular dystrophy that is characterized by recurrent erosions and stellate or thorn-like opacification located_in the cornea, hyaline and amyloid deposits in the stroma, and progressive vision loss later in life, and has_material_basis_in autosomal dominant inheritance of mutation of transforming growth factor beta-induced gene on chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased hyaline and amyloid protein deposition and disruption of the corneal surface."
    },
    "synonyms": [
        {
            "id": "DOID:0060444",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060444",
            "name": "CGD2",
            "description": ""
        },
        {
            "id": "DOID:0060444",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060444",
            "name": "avellino corneal dystrophy",
            "description": ""
        },
        {
            "id": "DOID:0060444",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060444",
            "name": "combined granular-lattice corneal dystrophy",
            "description": ""
        },
        {
            "id": "DOID:0060444",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060444",
            "name": "corneal dystrophy, Avellino type",
            "description": ""
        },
        {
            "id": "DOID:0060444",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060444",
            "name": "granular corneal dystrophy type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "granular corneal dystrophy type II",
            "description": "Type II granular corneal dystrophy (GCDII) is a rare form of stromal corneal dystrophy characterized by irregular-shaped well-demarcated granular deposits in the superficial central corneal stroma, and progressive visual impairment."
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "Avellino corneal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "CGD2",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "GCD2",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "GCDII",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "avellino corneal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "combined granular-lattice corneal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "granular corneal dystrophy type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "granular-lattice corneal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "ACD",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "CDA",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "combined granular-lattice corneal dystrophies",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "corneal dystrophy Avellino type",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "corneal dystrophy, AVELLINO type",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "granular and lattice corneal dystrophies",
            "description": ""
        },
        {
            "id": "MONDO:0011855",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011855",
            "name": "granular-lattice (Avellino) corneal dystrophy",
            "description": ""
        },
        {
            "id": "MIM:607541",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607541",
            "name": "Corneal dystrophy, Avellino type",
            "description": "Corneal dystrophy, Avellino type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060444"
    ],
    "unlinked_id_list": []
}