{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "lattice corneal dystrophy type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "LCD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "Lcd1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "lattice corneal dystrophy, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "corneal dystrophy, lattice type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "lattice corneal dystrophy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "classic lattice corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "Biber-Haab-Dimmer dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "CDL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "LCDI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "corneal dystrophy, lattice type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007380", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007380", 
            "name": "corneal dystrophy, lattice type I; Lcd1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:8943", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:8943", 
            "name": "familial amyloid neuropathy, Finnish type"
        }, 
        {
            "url": "https://www.omim.org/entry/122200", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:122200", 
            "name": "Corneal dystrophy, lattice type 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:8943", 
        "description": "An epithelial-stromal TGFBI dystrophy that is characterized by recurrent erosions and lattice line refractile and fleck-like opacification located_in the cornea, amyloid deposits beginning in the anterior 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 located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased amyloid protein deposition and disruption of the corneal surface.", 
        "resource": "Disease Ontology", 
        "id": "DOID:8943", 
        "name": "lattice corneal dystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/122200", 
            "id": "122200", 
            "database": "MIM"
        }
    ]
}