All diseases

OMIM ID
206100
OMIM term:
ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD
Alternative terms:

(∗) Location:
12q13.12  
(†) Associated OMIM genes:
SLC11A2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/rbddwz0w