Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Homozygous beta thalassemia
Frequent (30-79%)
Congenital syphilis
Frequent (30-79%)
Myelofibrosis
Occasional (5-29%)
Hereditary spherocytosis
Occasional (5-29%)
Alpha thalassaemia syndrome
Frequent (30-79%)
Thalassemia major
Frequent (30-79%)
Beta thalassemia intermedia
Frequent (30-79%)
Delta-4-3-oxosteroid-5-beta-reductase deficiency
Frequent (30-79%)
Carbonic anhydrase II deficiency
Myelosclerosis with myeloid metaplasia
Occasional (5-29%)
Dominant beta-thalassemia
Frequent (30-79%)
TARP syndrome
Occasional (5-29%)
Perinatal lethal bent bone dysplasia
Very frequent (80-99%)
Hydrops, lactic acidosis, sideroblastic anaemia, multisystemic failure syndrome
Always present (100%)
Leukocyte adhesion deficiency type III
Very rare (1-4%)
Related Symptoms
Quick Facts
- SNOMED CT
- 42952007
- UMLS CUI
- C2613439
- Fully Specified Name
- Extramedullary hematopoiesis (finding)
- Associated Conditions
- 15
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.