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Hemoglobin E disease

disorder
SNOMED 25065001CUI C0238159

Overview

Hemoglobin E 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
Hypochromia
Very frequent (80-99%)HP:0032231
Hypochromic, microcytic anaemia
Very frequent (80-99%)HP:0004840
Increased RBC count
Very frequent (80-99%)HP:0020059
Ineffective erythropoiesis
Very frequent (80-99%)HP:0010972
Microcytosis
Very frequent (80-99%)HP:0025066
Reduced HbA
Frequent (30-79%)HP:0011905
Drug-sensitive hemolytic anemia
Occasional (5-29%)HP:0004817
Increased red cell osmotic resistance
Occasional (5-29%)HP:0005546
Intrauterine growth retardation, IUGR
Occasional (5-29%)HP:0001511
Large spleen
Occasional (5-29%)HP:0001744
Premature birth
Occasional (5-29%)HP:0001622

Quick Facts

SNOMED CT
25065001
UMLS CUI
C0238159
Fully Specified Name
Hemoglobin E disease (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.