Immunodeficiency 39
Disease ID: disease_node_20015
Connections displayed (default: 10).
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| Dbxref | MIM:616345 |
|---|---|
| Subclassof | DOID_0050736, DOID_612 |
| Data Source | DOID |
| Synonyms | IMD39 |
| Doid Label | immunodeficiency 39 |
| Doid Description | A primary immunodeficiency disease characterized by impaired interferon I and III production in response to influenza virus infection that has_material_basis_in homozygous or compond heterozygous mutation in the IRF7 gene on chromosome 11p15.5. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_20015 |
| Doid Id | DOID_0111969 |
| Label | Immunodeficiency 39 |
- Outgoing r'ship
SUBCLASS_OFto/from Immunologic Deficiency Syndromes(ID:disease_node_4256) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)