 | |
Below is a table that brings to the attention all the known NCL disorders
and are represented by their gene and chromosome.
| Disease Name |
Gene ID |
Found on Chromosome |
| infantile NCL |
CLN1 |
1p32 |
| late infantile NCL |
CLN2 |
11p15 |
| Juvenile NCL |
CLN3 |
16p12 |
| Adult NCL (Kuffs) |
CLN4 |
Not Known |
| Finnish variant late infantile
NCL |
CLN5 |
13q31-32 |
| variant late infantile/early
juvenile NCL |
CLN6 |
15q21-23 |
| Turkish variant late infantile
NCL |
CLN7 |
Not Known |
| northern epilepsy |
CLN8 |
8p23 |
|
