{
    "disease_id": "DOID:0060444", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "granular corneal dystrophy type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "granular-lattice corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "avellino corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "CDA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "combined granular-lattice corneal dystrophies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "GCD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "corneal dystrophy Avellino type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "GCDII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "granular corneal dystrophy, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "granular-lattice (Avellino) corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "corneal dystrophy, AVELLINO type; CDA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "granular corneal dystrophy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "granular and lattice corneal dystrophies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "ACD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "corneal dystrophy, AVELLINO type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "combined granular-lattice corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011855", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011855", 
            "name": "CGD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060444", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060444", 
            "name": "CGD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060444", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060444", 
            "name": "avellino corneal dystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060444", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060444", 
            "name": "combined granular-lattice corneal dystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060444", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060444", 
            "name": "corneal dystrophy, Avellino type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060444", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060444", 
            "name": "granular corneal dystrophy type 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060444", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060444", 
        "name": "granular corneal dystrophy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060444#disease-associations", 
            "id": "0060444", 
            "database": "Alliance of Genome Resources"
        }
    ]
}