ABOVE is the twenty-four (24) hour day of CHROMOSOMIC CLOCK and this time is one (#1). 
Here I present: “Gelatinous Drop-like Corneal Dystrophy (GDCD)”, Victor McKusick, Mendelian Inheritance in Man’, 1966. Familial subepithelial corneal amyloidosis (FSCA), is an alternate term for gelatinous drop-like corneal dystrophy (GDCD).
INTRODUCTION.
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. A number of mutations causing this disease have been described in the gene encoding Tumor-associated calcium signal transducer 2 (TACSTD2). The TACSTD2 gene is on cytogenetic location 1p32.1 and genomic coordinates 1:58,575,433-58,577,252 . The screenshot of the TACSTD2 gene is shown BELOW of the 1,820 bp (base pairs) of DNA sequence length. 
