Related Conditions
Familial erythrocytosis due to diphosphoglycerate mutase deficiency(child)
Familial polycythemia vera(child)
High oxygen affinity hemoglobin polycythemia(child)
Chuvash polycythemia(child)
Autosomal recessive secondary polycythaemia not associated with Von Hippel Lindau gene(child)
Erythrocytosis(parent)
Hereditary red blood cell disorder(parent)
Quick Facts
- SNOMED CT
- 17342003
- UMLS CUI
- C0152264
- Fully Specified Name
- Familial erythrocytosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
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.