Preferred Name |
hereditary elliptocytosis |
|
Synonyms |
Congenital elliptocytosis ovalocytosis |
|
Definitions |
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. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
ID |
http://purl.obolibrary.org/obo/DOID_2373 |
|
comment |
Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
database_cross_reference |
ICD10CM:D58.1 UMLS_CUI:C0013902 MESH:D004612 SNOMEDCT_US_2023_03_01:154801000 ICD9CM:282.1 GARD:6621 MIM:130600 MIM:611804 NCI:C35882 ORDO:288 |
|
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. |
|
has exact synonym |
Congenital elliptocytosis ovalocytosis |
|
has_obo_namespace |
disease_ontology |
|
id |
DOID:2373 |
|
in_subset | ||
label |
hereditary elliptocytosis |
|
notation |
DOID:2373 |
|
prefLabel |
hereditary elliptocytosis |
|
subClassOf |