{
    "disease_id": "DOID:0060448", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007376", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007376", 
            "name": "Cfd"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007376", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007376", 
            "name": "Francois-Neetens speckled corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007376", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007376", 
            "name": "Franois-Neetens speckled corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007376", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007376", 
            "name": "corneal dystrophy, Francois-Neetens speckled or flecked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007376", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007376", 
            "name": "FranC'ois-Neetens speckled corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007376", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007376", 
            "name": "corneal dystrophy, FLECK"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007376", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007376", 
            "name": "FCD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060448", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060448", 
            "name": "FCD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060448", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060448", 
            "name": "Francois-Neetens speckled corneal dystrophy"
        }, 
        {
            "url": "https://www.omim.org/entry/121850", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:121850", 
            "name": "Corneal dystrophy, fleck"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060448", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060448", 
        "name": "Fleck corneal dystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/121850", 
            "id": "121850", 
            "database": "MIM"
        }
    ]
}