loading...| 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]. |
|
| alternative label |
Congenital elliptocytosis ovalocytosis |
|
| database_cross_reference |
ICD10CM:D58.1 OMIM:611804 UMLS_CUI:C0013902 MESH:D004612 SNOMEDCT_US_2023_03_01:154801000 ICD9CM:282.1 OMIM:130600 GARD:6621 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. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
| has exact synonym |
Congenital elliptocytosis ovalocytosis |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:2373 |
|
| in_subset | ||
| label |
hereditary elliptocytosis |
|
| notation |
DOID:2373 |
|
| note |
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]. |
|
| preferred label |
hereditary elliptocytosis |
|
| prefLabel |
hereditary elliptocytosis |
|
| subClassOf |