Essential thrombocythemia (clinical disorder)

disorder

SNOMED 109994006CUI C0040028

Overview

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

Treatments & Interventions

Interferon alfacon-1

substance

Interferon gamma-1b

substance

Interferon alfa-2a

substance

Interferon alfa-2b

substance

Hydroxyurea

substance

Peginterferon alfa-2b

substance

Peginterferon alfa-2a

substance

Signs & Symptoms

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

Abnormal shape of platelets

Very frequent (80-99%)HP:0011875

Abnormality of the cerebral blood vessels

Very frequent (80-99%)HP:0100659

Amaurosis fugax

Very frequent (80-99%)HP:0100576

Anomaly of the bone marrow cells

Very frequent (80-99%)HP:0005561

Blood clot in artery

Very frequent (80-99%)HP:0004420

Blood clot in vein

Very frequent (80-99%)HP:0004936

Blood platelet disease

Very frequent (80-99%)HP:0001872

Chest discomfort

Very frequent (80-99%)HP:0100749

Increased bleeding time

Very frequent (80-99%)HP:0003010

Increased megakaryocyte count

Very frequent (80-99%)HP:0005513

Megakaryocyte nucleus hyperlobulation

Very frequent (80-99%)HP:0031388

Myocardial infarction

Very frequent (80-99%)HP:0001658

Paresthesia

Very frequent (80-99%)HP:0003401

Thrombocythaemia

Very frequent (80-99%)HP:0001894

Tiredness

Very frequent (80-99%)HP:0012378

Bleeding tendency

Frequent (30-79%)HP:0001892

Dizziness

Frequent (30-79%)HP:0002321

Fragmented sleep

Frequent (30-79%)HP:0100785

Headache

Frequent (30-79%)HP:0002315

Large spleen

Frequent (30-79%)HP:0001744

Migraine headache

Frequent (30-79%)HP:0002076

Acute blood cancer

Occasional (5-29%)HP:0002488

Bruising susceptibility

Occasional (5-29%)HP:0000978

Erythromelalgia

Occasional (5-29%)HP:0032147

Hepatic venous thrombosis

Occasional (5-29%)HP:0030243

Hypoplastic myelodysplasia

Occasional (5-29%)HP:0002863

Impaired vision

Occasional (5-29%)HP:0000505

Increased total leukocyte count

Occasional (5-29%)HP:0001974

Myelofibrosis

Occasional (5-29%)HP:0011974

Transient ischemic attacks

Occasional (5-29%)HP:0002326

Related Conditions

Thrombocytosis(parent)

Malignant neoplasm of lymphatic and haemopoietic tissue(parent)

Disorder of hematopoietic morphology(parent)

Quick Facts

SNOMED CT: 109994006
UMLS CUI: C0040028
Fully Specified Name: Essential thrombocythemia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30
Known Treatments: 7

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.