All diseases

OMIM ID
300751
OMIM term:
ANEMIA, SIDEROBLASTIC, X-LINKED; XLSA
Alternative terms:
ANEMIA, HYPOCHROMIC; ANH1
ANEMIA, HEREDITARY SIDEROBLASTIC
HEREDITARY IRON-LOADING ANEMIA
(∗) Location:
Xp11.21  
(†) Associated OMIM genes:
ALAS2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/xrr4lqiy