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 OMIM:611804 UMLS_CUI:C0013902 MESH:D004612 SNOMEDCT_US_2020_03_01:154801000 ICD9CM:282.1 OMIM:130600 GARD:6621 NCI:C35882 ORDO:288 |
|
has exact synonym |
Congenital elliptocytosis ovalocytosis |
|
has_obo_namespace |
disease_ontology |
|
id |
DOID:2373 |
|
imported from | ||
in_subset | ||
label |
hereditary elliptocytosis |
|
notation |
DOID:2373 |
|
prefLabel |
hereditary elliptocytosis |
|
textual 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. |
|
subClassOf |
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