|
PPT1/CLN1
|
Infantile NCL
|
|
TPP1/CLN2
|
Late-infantile NCL
|
|
CLN3
|
Juvenile NCL
|
|
DNAJC5/CLN4
|
Adult-onset NCL, Kufs disease, Parry disease
|
|
CLN5
|
Late-infantile NCL (Finnish variant)
|
|
CLN6
|
Variant late-infantile NCL
|
|
MFSD8/CLN7
|
Late-infantile NCL (Turkish variant)
|
|
CLN8
|
Northern epilepsy (epilespy, progressive with mental retardation, EPMR)
|
|
CTSD/CLN10
|
Congenital, neonatal and late infantile NCL
|
|
PGRN/CLN11
|
Adult-onset NCL, frontotemporal dementia in heterozygotes
|
|
ATP13A2/CLN12
|
Juvenile-onset NCL
|
|
CTSF/CLN13
|
Adult-onset NCL
|
|
KCTD7/CLN14
|
Infantile NCL
|
