Iga Deficiency
Disease ID: disease_node_9044
Connections displayed (default: 10).
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| Dbxref | GARD:10197, MESH:D017098, MIM:137100, MIM:269650, MIM:609529, ORDO:69127, SNOMEDCT_US_2023_03_01:29260007, UMLS_CUI:C0162538 |
|---|---|
| Subclassof | DOID_0050737, DOID_2115 |
| Data Source | DOID, MESH |
| Synonyms | IgA deficiency, gamma-A-globulin deficiency |
| Mesh Id | D017098 |
| Mesh Label | IgA Deficiency |
| Mesh Subclassof | D004406 |
| Doid Label | immunoglobulin alpha deficiency |
| Doid Description | A B cell deficiency that is an autosomal recessive disorder that has_material_basis_in mutation in the IgA (CD79 alpha) antigen receptor. Xref MGI. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_9044 |
| Doid Id | DOID_0060025 |
| Label | Iga Deficiency |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from B Cell Deficiency(ID:disease_node_17331) (Disease)