IRIDA (Iron-refractory iron deficiency anemia) syndrome is a rare autosomal recessive iron metabolism disorder characterized by iron deficiency anemia (hypochromic, microcytic) that is often unresponsive to oral iron intake and partially responsive to parenteral iron treatment.
Synonyms: Iron-refractory iron deficiency anemia
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Term information
database cross reference
- ICD-10:D50.8 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- UMLS:C0085576 (E (Exact mapping: the two concepts are equivalent))
- OMIM:206200 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:D50.8 (Attributed (The ICD10 code is attributed by Orphanet))
Term relations
Subclass of:
- disease
- present_in some Worldwide and has_point_prevalence_range some <1 / 1 000 000
- present_in some Worldwide and has_cases/families_value value 75.0
- has_inheritance some autosomal recessive
- part_of some Constitutional anemia due to iron metabolism disorder
- has_age_of_onset some infancy
- has_age_of_onset some neonatal