Agammaglobulinemia 10
Disease ID: disease_node_17352
Connections displayed (default: 10).
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| Dbxref | MIM:619707 |
|---|---|
| Subclassof | DOID_0050736, DOID_2583 |
| Data Source | DOID |
| Doid Label | agammaglobulinemia 10 |
| Doid Description | An agammaglobulinemia that is characterized by early-childhood onset of recurrent viral and bacterial infections affecting various organ systems, particularly the sinopulmonary system. and that has_material_basis_in heterozygous mutation in the SPI1 gene on chromosome 11p11. |
| Existence Starts During | HP_0011463 |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17352 |
| Doid Id | DOID_0081142 |
| Label | Agammaglobulinemia 10 |
- Outgoing r'ship
SUBCLASS_OFto/from Agammaglobulinemia(ID:disease_node_1066) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)