All diseases

OMIM ID
256730
OMIM term:
CEROID LIPOFUSCINOSIS, NEURONAL, 1; CLN1
Alternative terms:
CEROID LIPOFUSCINOSIS, NEURONAL, 1, VARIABLE AGE AT ONSET NEURONAL CEROID LIPOFUSCINOSIS, INFANTILE, INCLUDED; INCL, INCLUDED
SANTAVUORI DISEASE, INCLUDED
SANTAVUORI-HALTIA DISEASE, INCLUDED
(∗) Location:
1p34.2  
(†) Associated OMIM genes:
PPT1  
(‡) Associated MGI genes:
Ppt1  

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