All diseases

OMIM ID
137440
OMIM term:
GERSTMANN-STRAUSSLER DISEASE; GSD
Alternative terms:
ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE
GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS
CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS
AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY
PRION DEMENTIA
(∗) Location:
20p13  
(†) Associated OMIM genes:
PRNP  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/abqo38j5