Search Ontology:
Human Disease
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
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- 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 )
- is a type of
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Genes Involved
Zebrafish Models