All diseases

OMIM ID
253300
OMIM term:
SPINAL MUSCULAR ATROPHY, TYPE I; SMA1
Alternative terms:
SMA I
SMA, INFANTILE ACUTE FORM
MUSCULAR ATROPHY, INFANTILE
WERDNIG-HOFFMANN DISEASE
(∗) Location:
5q13.2  
(†) Associated OMIM genes:
SMN1  
(‡) Associated MGI genes:
Smn1   Vps54  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/gzh0b9yv