- OMIM ID
-
206200
- OMIM term:
- IRON-REFRACTORY IRON DEFICIENCY ANEMIA; IRIDA
- Alternative terms:
-
ANEMIA, HYPOCHROMIC MICROCYTIC, WITH DEFECT IN IRON METABOLISM
IRON-HANDLING DISORDER, HEREDITARY
PSEUDO-IRON-DEFICIENCY ANEMIA
- (∗) Location:
- 22q12.3
- (†) Associated OMIM genes:
- TMPRSS6
- (‡) Associated MGI genes:
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