{
    "disease_id": "DOID:0060448",
    "recommended_name": {
        "id": "DOID:0060448",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060448",
        "name": "Fleck corneal dystrophy",
        "description": "A stromal dystrophy that is characterized by numerous tiny, dot-like white flecks scattered in all layers of the corneal stroma and that has_material_basis_in heterozygous mutation in the PIKFYVE gene on chromosome 2q34."
    },
    "synonyms": [
        {
            "id": "DOID:0060448",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060448",
            "name": "FCD",
            "description": ""
        },
        {
            "id": "DOID:0060448",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060448",
            "name": "Francois-Neetens speckled corneal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007376",
            "name": "fleck corneal dystrophy",
            "description": "Fleck corneal dystrophy (FCD) is a rare generally asymptomatic form of stromal corneal dystrophy characterized by multiple asymptomatic, non-progressive opacities disseminated throughout the corneal stroma with no effect on visual acuity."
        },
        {
            "id": "MONDO:0007376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007376",
            "name": "FCD",
            "description": ""
        },
        {
            "id": "MONDO:0007376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007376",
            "name": "fleck corneal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007376",
            "name": "Cfd",
            "description": ""
        },
        {
            "id": "MONDO:0007376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007376",
            "name": "Francois-Neetens speckled corneal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007376",
            "name": "Franois-Neetens speckled corneal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007376",
            "name": "corneal dystrophy, Francois-Neetens speckled or flecked",
            "description": ""
        },
        {
            "id": "MONDO:0007376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007376",
            "name": "FranC'ois-Neetens speckled corneal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007376",
            "name": "corneal fleck dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007376",
            "name": "corneal dystrophy, FLECK",
            "description": ""
        },
        {
            "id": "MIM:121850",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/121850",
            "name": "Corneal dystrophy, fleck",
            "description": "Corneal dystrophy, fleck"
        }
    ]
}