Autosomal recessive common variable immunodeficiency due to complement C3d receptor 2 mutation (disorder)
| Code | 1351961009 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | primitive |
| Effective time | 20241201 |
85995004Autosomal recessive hereditary disorder
disorder
191010004Common variable immunodeficiency
disorder
363138005Hereditary disorder of immune system
disorder
None (leaf concept).