Anemia, Hemolytic, Congenital
Disease ID: disease_node_1187
Connections displayed (default: 10).
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| Dbxref | GARD:6167, ICD10CM:D58.9, ICD9CM:282, MESH:D000745, NCI:C34379, SNOMEDCT_US_2023_03_01:42601008, UMLS_CUI:C0002881 |
|---|---|
| Subclassof | DOID_0080015, DOID_583 |
| Data Source | DOID, MESH |
| Synonyms | congenital hemolytic anaemia, hereditary hemolytic anaemia, hereditary hemolytic anemia |
| Mesh Id | D000745 |
| Mesh Label | Anemia, Hemolytic, Congenital |
| Mesh Subclassof | D030342, D000743 |
| Doid Label | congenital hemolytic anemia |
| Existence Starts During | HP_0003577 |
| Disease Node Id | disease_node_1187 |
| Doid Id | DOID_589 |
| Disease Has Basis In | HP_0001197 |
| Label | Anemia, Hemolytic, Congenital |
- Incoming r'ship
SUBCLASS_OFto/from X-Linked Congenital Hemolytic Anemia(ID:disease_node_15282) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Spherocytosis, Hereditary(ID:disease_node_7020) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hemoglobinopathies(ID:disease_node_3811) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Anemia, Hemolytic(ID:disease_node_1184) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Anemia, Hemolytic, Congenital Nonspherocytic(ID:disease_node_1189) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Physical Disorder(ID:disease_node_13159) (Disease)