anemia, sideroblastic, Pyridoxine-Refractory, autosomal recessive

Preferred Label : anemia, sideroblastic, Pyridoxine-Refractory, autosomal recessive;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0567445;

UMLS CUI

C2673914;

Currated CISMeF NLP mapping
- Adult-onset autosomal recessive sideroblastic anemia [ORDO Disease]
- Adult-onset autosomal recessive sideroblastic anemia (disorder) [SNOMED CT concept]
- Anemia, sideroblastic, 2, pyridoxine-refractory [OMIM Phenotype]
- Autosomal recessive sideroblastic anaemia, pyridoxine-refractory [ICD-11 More detail]
- autosomal recessive pyridoxine-refractory sideroblastic anemia 2 [DO Concept]
Related record
- anemia, sideroblastic, Pyridoxine-Refractory, autosomal recessive [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Adult-onset autosomal recessive sideroblastic anemia [ORDO Disease]