Elliptocytosis, Hereditary
Disease ID: disease_node_2759
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| Dbxref | 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 |
|---|---|
| Subclassof | DOID_74 |
| Data Source | DOID, MESH |
| Synonyms | Congenital elliptocytosis, ovalocytosis |
| Mesh Id | D004612 |
| Mesh Label | Elliptocytosis, Hereditary |
| Mesh Subclassof | D000745 |
| Doid Label | hereditary elliptocytosis |
| Doid Description | 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]. |
| Disease Node Id | disease_node_2759 |
| Doid Id | DOID_2373 |
| Label | Elliptocytosis, Hereditary |
- Outgoing r'ship
SUBCLASS_OFto/from Hematologic Diseases(ID:disease_node_3773) (Disease)