All diseases

OMIM ID
123400
OMIM term:
CREUTZFELDT-JAKOB DISEASE; CJD
Alternative terms:
CREUTZFELDT-JAKOB DISEASE, FAMILIAL CREUTZFELDT-JAKOB DISEASE, SPORADIC, INCLUDED; sCJD, INCLUDED
CREUTZFELDT-JAKOB DISEASE, VARIANT, INCLUDED; vCJD, INCLUDED
CREUTZFELDT-JAKOB DISEASE, HEIDENHAIN VARIANT, INCLUDED
(∗) Location:
20p13   6p21.32  
(†) Associated OMIM genes:
HLA-DQB1   PRNP  
(‡) Associated MGI genes:
Prnp  

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