Spherocytosis, Hereditary
Disease ID: disease_node_7020
Connections displayed (default: 10).
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| Dbxref | GARD:6639, ICD10CM:D58.0, ICD9CM:282.0, MESH:D013103, NCI:C97074, ORDO:822, SNOMEDCT_US_2023_03_01:154795009, UMLS_CUI:C0037889 |
|---|---|
| Subclassof | DOID_589 |
| Data Source | DOID, MESH |
| Synonyms | Congenital spherocytic hemolytic anemia, Minkowski Chauffard syndrome, spherocytic anemia |
| Mesh Id | D013103 |
| Mesh Label | Spherocytosis, Hereditary |
| Mesh Subclassof | D000745 |
| Doid Label | hereditary spherocytosis |
| Doid Description | A congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape. Xref MGI. |
| Disease Node Id | disease_node_7020 |
| Doid Id | DOID_12971 |
| Label | Spherocytosis, Hereditary |
- Outgoing r'ship
SUBCLASS_OFto/from Anemia, Hemolytic, Congenital(ID:disease_node_1187) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hereditary Spherocytosis Type 3(ID:disease_node_15279) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hereditary Spherocytosis Type 2(ID:disease_node_15280) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hereditary Spherocytosis Type 1(ID:disease_node_15281) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hereditary Spherocytosis Type 5(ID:disease_node_15277) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hereditary Spherocytosis Type 4(ID:disease_node_15278) (Disease)