All diseases

OMIM ID
605280
OMIM term:
SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT; SPG13
Alternative terms:

(∗) Location:
2q33.1  
(†) Associated OMIM genes:
HSPD1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/7kfluiu0