B Cell Deficiency
Disease ID: disease_node_17331
Connections displayed (default: 10).
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| Dbxref | ICD9CM:279.03, SNOMEDCT_US_2023_03_01:190982008, UMLS_CUI:C0154276 |
|---|---|
| Subclassof | DOID_612 |
| Data Source | DOID |
| Synonyms | B cell (antibody) deficiencies, Immunoglobulin heavy chain deficiency, immunoglobulin heavy chain deletion |
| Doid Label | B cell deficiency |
| Doid Description | A primary immunnodeficiency disease that is caused by a lack of infection-fighting antibody producing B cells (immunoglobulins) or B cells that are not functioning properly. |
| Disease Node Id | disease_node_17331 |
| Doid Id | DOID_2115 |
| Label | B Cell Deficiency |
| Doid Alternate Ids | DOID_6026 |
- Incoming r'ship
SUBCLASS_OFto/from Selective Immunoglobulin Deficiency Disease(ID:disease_node_17332) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Lambda 5 Deficiency(ID:disease_node_17348) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Immunodeficiency 62(ID:disease_node_17346) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Iga Deficiency(ID:disease_node_9044) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hyperimmunoglobulin Syndrome(ID:disease_node_17336) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Immunoglobulin Beta Deficiency(ID:disease_node_17347) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Congenital Hypogammaglobulinemia(ID:disease_node_17345) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Immunologic Deficiency Syndromes(ID:disease_node_4256) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Agammaglobulinemia(ID:disease_node_1066) (Disease)