IRIDA syndrome
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. [ Orphanet:209981 ]
Term info
- OMIM:206200 (Orphanet:209981/e)
- GARD:0010957 (MONDO:equivalentTo)
- SCTID:722005000 (MONDO:equivalentTo)
- Orphanet:209981 (OMIM:206200)
- MESH:C562385 (MONDO:equivalentTo)
ordo_disease
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.
https://omim.org/entry/206200, http://purl.obolibrary.org/obo/Orphanet_209981, http://identifiers.org/mesh/C562385, http://identifiers.org/snomedct/722005000
iron-refractory iron deficiency anemia, IRIDA syndrome
anemia, hypochromic microcytic, with defect in iron metabolism, iron-handling disorder, hereditary, pseudo-iron-deficiency Anemia, IRIDA
MONDO:0008788