All diseases

OMIM ID
242900
OMIM term:
IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE
Alternative terms:

(∗) Location:
2q35  
(†) Associated OMIM genes:
SMARCAL1  
(‡) Associated MGI genes:
Smarcal1  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/4ncsl2vb