Overview
Poikilocytosis is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Congenital erythropoietic porphyria
Occasional (5-29%)
Congenital dyserythropoietic anemia, type III
Very frequent (80-99%)
HNSHA due to glucose phosphate isomerase deficiency
Occasional (5-29%)
Myelofibrosis
Occasional (5-29%)
Congenital dyserythropoietic anemia, type I
Hereditary orotic aciduria, type 1
Deficiency of phosphoenolpyruvate kinase
Occasional (5-29%)
Congenital porphyria
Occasional (5-29%)
Hereditary ovalocytosis
Occasional (5-29%)
Glucose phosphate isomerase deficiency
Occasional (5-29%)
Myelosclerosis with myeloid metaplasia
Occasional (5-29%)
Congenital dyserythropoietic anemia type IV
Always present (100%)
X-linked sideroblastic anemia with spinocerebellar ataxia
Occasional (5-29%)
Iron-refractory iron deficiency anemia
X-linked congenital dyserythropoietic anemia with thrombocytopenia
Very frequent (80-99%)
Fibrosis, neurodegeneration, cerebral angiomatosis syndrome
Quick Facts
- SNOMED CT
- 165479004
- UMLS CUI
- C0221281
- Fully Specified Name
- Poikilocytosis (finding)
- Associated Conditions
- 16
- 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.