{
    "disease_id": "DOID:0060449", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "primary familial amyloidosis of the cornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "subepithelial amyloidosis of the cornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "lattice corneal dystrophy type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "amyloidosis corneal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "GDCD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "corneal dystrophy, gelatinous drop-like; GDLD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "amyloid corneal dystrophy, Japanese type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "CDGDL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "lattice corneal dystrophy, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "corneal dystrophy, lattice type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "corneal dystrophy, gelatinous drop-like"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "amyloidosis, corneal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "corneal amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008777", 
            "name": "GDLD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060449", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060449", 
            "name": "GDCD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060449", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060449", 
            "name": "corneal amyloidosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060449", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060449", 
            "name": "primary familial amyloidosis of the cornea"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060449", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060449", 
            "name": "subepithelial amyloidosis of the cornea"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060449", 
        "description": "An epithelial and subepithelial dystrophy that is characterized by severe corneal amyloidosis leading to blindness and that has_material_basis_in homozygous or compound heterozygous mutation in the TACSTD2 gene which encodes the monoclonal antibody-defined, tumor-associated antigen GA733-1, on chromosome 1p32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060449", 
        "name": "gelatinous drop-like corneal dystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060449#disease-associations", 
            "id": "0060449", 
            "database": "Alliance of Genome Resources"
        }
    ]
}