All diseases

OMIM ID
182600
OMIM term:
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A
Alternative terms:
SPG3
STRUMPELL DISEASE
FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1
(∗) Location:
14q22.1  
(†) Associated OMIM genes:
ATL1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/1rt5n57y