Agammaglobulinemia 8B
Disease ID: disease_node_17351
Connections displayed (default: 10).
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| Dbxref | MIM:619824 |
|---|---|
| Subclassof | DOID_2583, DOID_0050737 |
| Data Source | DOID |
| Doid Label | agammaglobulinemia 8B |
| Doid Description | An agammaglobulinemia that is characterized by onset of recurrent infections in early childhood and that has_material_basis_in homozygous loss-of-function mutation in the TCF3 gene on chromosome 19p13. |
| Existence Starts During | HP_0011463 |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17351 |
| Doid Id | DOID_0081143 |
| Label | Agammaglobulinemia 8B |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Agammaglobulinemia(ID:disease_node_1066) (Disease)