Iron-refractory iron deficiency anemia

disorder

SNOMED 722005000CUI C0085576

Overview

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

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Hypochromic, microcytic anaemia

Very frequent (80-99%)HP:0004840

Iron-deficiency anaemia

Very frequent (80-99%)HP:0001891

Microcytosis

Very frequent (80-99%)HP:0025066

Decreased circulating iron concentration

Frequent (30-79%)HP:0040303

Decreased transferrin saturation

Frequent (30-79%)HP:0012464

Elevated circulating hepcidin concentration

Frequent (30-79%)HP:0031877

Anemic pallor

Occasional (5-29%)HP:0001017

Inflammation of oral commisures

Occasional (5-29%)HP:0030318

Concave nail

Very rare (1-4%)HP:0001598

Hair loss

Very rare (1-4%)HP:0001596

Anisocytosis

HP:0011273

Poikilocytosis

HP:0004447

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Iron deficiency anemia(parent)

Quick Facts

SNOMED CT: 722005000
UMLS CUI: C0085576
Fully Specified Name: Iron-refractory iron deficiency anemia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.