Hemoglobin E/beta thalassemia disease

disorder

SNOMED 234392002CUI C0472777

Overview

Hemoglobin E/beta thalassemia disease is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Abnormal Hb

Very frequent (80-99%)HP:0011902

Immune deficiency

Very frequent (80-99%)HP:0002721

Low number of red blood cells or haemoglobin

Very frequent (80-99%)HP:0001903

Hyperferritinemia

Frequent (30-79%)HP:0003281

Related Conditions

Haemoglobin E beta plus thalassaemia(child)

Hemoglobin E beta zero thalassemia(child)

Hemoglobin E disease(parent)

Beta thalassemia(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 234392002
UMLS CUI: C0472777
Fully Specified Name: Hemoglobin E/beta thalassemia disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 4

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.