All diseases

OMIM ID
254900
OMIM term:
EPILEPSY, PROGRESSIVE MYOCLONIC 4, WITH OR WITHOUT RENAL FAILURE; EPM4
Alternative terms:
ACTION MYOCLONUS-RENAL FAILURE SYNDROME; AMRF
MYOCLONUS-NEPHROPATHY SYNDROME
(∗) Location:
4q21.1  
(†) Associated OMIM genes:
SCARB2  
(‡) Associated MGI genes:

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