All diseases

OMIM ID
235200
OMIM term:
HEMOCHROMATOSIS; HFE
Alternative terms:
HLAH
HEMOCHROMATOSIS, HEREDITARY; HH
(∗) Location:
20p12.3   6p22.2  
(†) Associated OMIM genes:
BMP2   HFE  
(‡) Associated MGI genes:
B2m   Heph   Hfe   Hmox1  

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* quick link - http://q.sanger.ac.uk/ngke99t5