{
    "disease_id": "DOID:0060449",
    "recommended_name": {
        "id": "DOID:0060449",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060449",
        "name": "gelatinous drop-like corneal dystrophy",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060449",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060449",
            "name": "GDCD",
            "description": ""
        },
        {
            "id": "DOID:0060449",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060449",
            "name": "corneal amyloidosis",
            "description": ""
        },
        {
            "id": "DOID:0060449",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060449",
            "name": "primary familial amyloidosis of the cornea",
            "description": ""
        },
        {
            "id": "DOID:0060449",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060449",
            "name": "subepithelial amyloidosis of the cornea",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "gelatinous drop-like corneal dystrophy",
            "description": "Gelatinous drop-like corneal dystrophy (GDCD) is a form of superficial corneal dystrophy characterized by multiple prominent milky-white gelatinous nodules beneath the corneal epithelium, and marked visual impairment."
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "GDCD",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "corneal amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "gelatinous drop-like corneal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "primary familial amyloidosis of the cornea",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "subepithelial amyloidosis of the cornea",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "CDGDL",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "GDLD",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "amyloid corneal dystrophy, Japanese type",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "amyloidosis corneal",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "corneal dystrophy, gelatinous drop-like",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "corneal dystrophy, lattice type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008777",
            "name": "lattice corneal dystrophy type 3",
            "description": ""
        },
        {
            "id": "MIM:204870",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/204870",
            "name": "Corneal dystrophy, gelatinous drop-like",
            "description": "Corneal dystrophy, gelatinous drop-like"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060449"
    ],
    "unlinked_id_list": []
}