All diseases

OMIM ID
204200
OMIM term:
CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3
Alternative terms:
NEURONAL CEROID LIPOFUSCINOSIS, JUVENILE; JNCL
BATTEN DISEASE
VOGT-SPIELMEYER DISEASE
SPIELMEYER-SJOGREN DISEASE
(∗) Location:
16p11.2  
(†) Associated OMIM genes:
CLN3  
(‡) Associated MGI genes:
Clcn3   Clcn6   Cln3   Ppt1  

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