Preferred Name |
hereditary elliptocytosis |
|
Synonyms |
|
|
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]. |
|
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. |
|
hasDbXref |
SNOMEDCT_US_2016_03_01:191169008 NCI:C36293 ORDO:288 SNOMEDCT_US_2016_03_01:267558001 UMLS_CUI:C0013902 SNOMEDCT_US_2016_03_01:178935009 OMIM:130600 SNOMEDCT_US_2016_03_01:154801000 NCI:C35882 OMIM:611804 ICD9CM:282.1 ICD10CM:D58.1 SNOMEDCT_US_2016_03_01:58864003 MESH:D004612 |
|
hasExactSynonym |
Congenital elliptocytosis ovalocytosis |
|
hasOBONamespace |
disease_ontology |
|
id |
DOID:2373 |
|
imported from | ||
inSubset | ||
label |
hereditary elliptocytosis |
|
prefixIRI |
DOID:2373 |
|
prefLabel |
hereditary elliptocytosis |
|
subClassOf |
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