Immunodeficiency 79
Disease ID: disease_node_20010
Connections displayed (default: 10).
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| Dbxref | MIM:619238 |
|---|---|
| Subclassof | DOID_11200, DOID_0050737 |
| Data Source | DOID |
| Synonyms | IMD79 |
| Doid Label | immunodeficiency 79 |
| Doid Description | A T cell deficiency characterized by childhood onset of recurrent and recalcitrant skin warts due to uncontrolled viral infection with human papillomavirus and absence of the CD4 antigen on T cells, monocytes, and dendritic cells that has_material_basis_in homozygous or compound heterozygous mutation in CD4 on chromosome 12p13. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_20010 |
| Doid Id | DOID_0112277 |
| Label | Immunodeficiency 79 |
- Outgoing r'ship
SUBCLASS_OFto/from T Cell Deficiency(ID:disease_node_20002) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)