All diseases

OMIM ID
256731
OMIM term:
CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5
Alternative terms:
CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSET NEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED
FINNISH vLINCL, INCLUDED
(∗) Location:
13q22.3  
(†) Associated OMIM genes:
CLN5  
(‡) Associated MGI genes:
Cln5  

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