All diseases

OMIM ID
159950
OMIM term:
SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY; SMAPME
Alternative terms:

(∗) Location:
8p22  
(†) Associated OMIM genes:
ASAH1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/km3imdvi