All diseases

OMIM ID
600886
OMIM term:
HYPERFERRITINEMIA-CATARACT SYNDROME
Alternative terms:

(∗) Location:
19q13.33  
(†) Associated OMIM genes:
FTL  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/89whqub7