Common Variable Immunodeficiency
Disease ID: disease_node_9017
Connections displayed (default: 10).
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| Dbxref | GARD:6140, ICD10CM:D83, ICD9CM:279.06, MESH:D017074, MIM:PS607594, ORDO:1572, SNOMEDCT_US_2023_03_01:191010004, UMLS_CUI:C0009447 |
|---|---|
| Subclassof | DOID_2583, DOID_0050737, DOID_417 |
| Data Source | DOID, MESH |
| Synonyms | CVID, acquired agammaglobulinemia, acquired hypogammaglobulinemia, common variable agammaglobulinemia, sporadic hypogammaglobulinemia |
| Mesh Id | D017074 |
| Mesh Label | Common Variable Immunodeficiency |
| Mesh Subclassof | D007153 |
| Doid Label | common variable immunodeficiency |
| Doid Description | An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
| Has Phenotype | HP_0004313 |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_9017 |
| Doid Id | DOID_12177 |
| Label | Common Variable Immunodeficiency |
- Outgoing r'ship
SUBCLASS_OFto/from Agammaglobulinemia(ID:disease_node_1066) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 1(ID:disease_node_17328) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 2(ID:disease_node_17327) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 8(ID:disease_node_17321) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 14(ID:disease_node_17316) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 12(ID:disease_node_17318) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autoimmune Disease(ID:disease_node_14242) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 6(ID:disease_node_17323) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 7(ID:disease_node_17322) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 5(ID:disease_node_17324) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 4(ID:disease_node_17325) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 10(ID:disease_node_17320) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 13(ID:disease_node_17317) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 11(ID:disease_node_17319) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Common Variable Immunodeficiency 3(ID:disease_node_17326) (Disease)