All diseases

OMIM ID
604360
OMIM term:
SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11
Alternative terms:
SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT AND THIN CORPUS CALLOSUM
SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUS CALLOSUM
HSP-TCC
(∗) Location:
15q21.1  
(†) Associated OMIM genes:
SPG11  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/xeid182y