| DISEASE NAME | Common variable immunodeficiency |
| DISEASE CATEGORY (ICD10) | Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism |
| DISEASE ID (ICD10) | D83.8 |
| DISEASE ID (OMIM) | 146830; 240500; 607594; 613493; 613494; 613495; 613496; 614699; 615577; 616576 |
| 11 combinations linked to 1572 | OLI076; OLI1711; OLI1712; OLI1713; OLI1714; OLI1715; OLI1716; OLI1717; OLI1718; OLI1719; OLI1720 |
| 11 gene combinations linked to 1572 | PSTPIP1; TNFSF11; CD8A; PIK3R1; TNFRSF13B; LRBA; MYSM1; PIK3CD; IL17RA; MYSM1; IL21R; TAP1; NCF2; TCIRG1; TIRAP; IL10RA; TIRAP; IGLL1; TBK1; IL10RA; IL10RB; LRBA; GATA2; KMT2D; NFKB1; STAT5B; TFRC; TCF3; TNFRSF13B |
| ORPHANET ID | 1572 |