All diseases

OMIM ID
270685
OMIM term:
SPASTIC PARAPLEGIA 17; SPG17
Alternative terms:
SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET
SILVER SYNDROME
SILVER SPASTIC PARAPLEGIA SYNDROME
(∗) Location:
11q12.3  
(†) Associated OMIM genes:
BSCL2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/p0y3hsey