Overview
Familial thrombocytosis 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.
Bleeding tendency
Very frequent (80-99%)HP:0001892
Blood clot in artery
Very frequent (80-99%)HP:0004420
Blood clot in vein
Very frequent (80-99%)HP:0004936
Increased platelet count
Very frequent (80-99%)HP:0001894
Cerebrovascular ischemia
Frequent (30-79%)HP:0002637
Chest discomfort
Frequent (30-79%)HP:0100749
Headache
Frequent (30-79%)HP:0002315
Large spleen
Frequent (30-79%)HP:0001744
Occlusive vascular disease
Frequent (30-79%)HP:0004950
Paresthesia
Frequent (30-79%)HP:0003401
Profuse sweating
Frequent (30-79%)HP:0000975
Skin itching
Frequent (30-79%)HP:0000989
Transient ischemic attacks
Frequent (30-79%)HP:0002326
Acute myeloid leukaemia
Occasional (5-29%)HP:0004808
Chronic myeloid leukemia
Occasional (5-29%)HP:0005506
Difficulty articulating speech
Occasional (5-29%)HP:0001260
Dizziness
Occasional (5-29%)HP:0002321
Epilepsy
Occasional (5-29%)HP:0001250
Hypoplastic myelodysplasia
Occasional (5-29%)HP:0002863
Partial loss of field of vision
Occasional (5-29%)HP:0001123
Pulmonary artery hypertension
Occasional (5-29%)HP:0002092
Syncope
Occasional (5-29%)HP:0001279
Weight loss
Occasional (5-29%)HP:0001824
Related Conditions
Quick Facts
- SNOMED CT
- 720950009
- UMLS CUI
- C4303761
- Fully Specified Name
- Familial thrombocytosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 23
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.