Microcytic anemia

disorder

SNOMED 234349007CUI C5194182

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Congenital transferrin deficiency(child)

Microcytic normochromic anemia(child)

Microcytic hypochromic anemia(child)

Haemolytic disease of foetus OR newborn due to isoimmunisation(child)

Early-onset neurodegeneration, choreoathetoid movement, microcytic anaemia due to IREB2 mutation(child)

Anemia(parent)

Quick Facts

SNOMED CT: 234349007
UMLS CUI: C5194182
Fully Specified Name: Microcytic anemia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.