hereditary elliptocytosis

Term ID

DOID:2373

Synonyms

• Congenital elliptocytosis
• ovalocytosis

Definition

A hematopoietic system disease characterized by oval or elliptical red blood cells, slight or absent hemolysis with little or no anemia; splenomegaly is often present. (3)

References

• GARD:6621
• ICD10CM:D58.1
• ICD9CM:282.1
• MESH:D004612
• MIM:130600
• MIM:611804
• NCI:C35882
• ORDO:288
• SNOMEDCT_US_2023_03_01:154801000
• UMLS_CUI:C0013902

Ontology

Human Disease   ( DOID:2373 )