All diseases

OMIM ID
609820
OMIM term:
ERYTHROCYTOSIS, FAMILIAL, 3; ECYT3
Alternative terms:

(∗) Location:
1q42.2  
(†) Associated OMIM genes:
EGLN1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/681dxmld