All diseases

OMIM ID
604218
OMIM term:
ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB
Alternative terms:

(∗) Location:
3q26.1  
(†) Associated OMIM genes:
SERPINI1  
(‡) Associated MGI genes:
Serpini1  

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* quick link - http://q.sanger.ac.uk/sbog5j9f