Southeast Asian ovalocytosis

disorder

SNOMED 723623002CUI C1862322

Overview

Southeast Asian ovalocytosis 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.

Anemic pallor

Frequent (30-79%)HP:0001017

Elliptocyte

Frequent (30-79%)HP:0004445

Hemolytic anaemia

Frequent (30-79%)HP:0001878

Increased lactate dehydrogenase level

Frequent (30-79%)HP:0025435

Large spleen

Frequent (30-79%)HP:0001744

Polychromasia on peripheral blood smear

Frequent (30-79%)HP:0034609

Poor exercise tolerance

Frequent (30-79%)HP:0003546

Red cell stomatocytosis

Frequent (30-79%)HP:0004446

Reduced haptoglobin level

Frequent (30-79%)HP:0020181

Reticulocytosis

Frequent (30-79%)HP:0001923

Tiredness

Frequent (30-79%)HP:0012378

Unconjugated hyperbilirubinemia

Frequent (30-79%)HP:0008282

Yellowing of the skin

Frequent (30-79%)HP:0000952

Increased MCV

Occasional (5-29%)HP:0005518

Renal tubular acidosis

Occasional (5-29%)HP:0001947

Spherocytosis

Occasional (5-29%)HP:0004444

Related Conditions

Autosomal dominant hereditary disorder(parent)

Erythrocyte enzyme deficiency(parent)

Stomatocytosis(parent)

Hereditary red blood cell disorder(parent)

Quick Facts

SNOMED CT: 723623002
UMLS CUI: C1862322
Fully Specified Name: Southeast Asian ovalocytosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 16

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.