Loading disease data
| Disease | Prevalence | Drugs | Proteins | |
|---|---|---|---|---|
| Immunodeficiency 31A (IMD31A) | Ultra-Rare | 5 | 2 | |
| Immunodeficiency 31B (IMD31B) | N/A | — | 2 | |
| Immunodeficiency 67 (IMD67) | Ultra-Rare | — | 2 | |
| Autoimmune disease 6 (AIS6) | N/A | 15 | 1 | |
| Autoimmune disease, multisystem, infantile-onset, 1 (ADMIO1) | Ultra-Rare | — | 1 | |
| Autoimmune disease, multisystem, infantile-onset, 2 (ADMIO2) | N/A | — | 1 | |
| Autoimmune disease, multisystem, infantile-onset, 5 (ADMIO5) | N/A | — | 1 | |
| Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant (AIPDSA) | N/A | — | 1 | |
| Autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessive (AIPDSB) | Ultra-Rare | — | 1 | |
| C1q deficiency 2 (C1QD2) | N/A | — | 1 | |
| Complement component 2 deficiency (C2D) | N/A | — | 1 | |
| Complement component 6 deficiency (C6D) | N/A | — | 1 | |
| Complement component 7 deficiency (C7D) | N/A | — | 1 | |
| Complement component C1s deficiency (C1SD) | N/A | — | 1 | |
| Complement factor B deficiency (CFBD) | N/A | — | 1 | |
| Ectodermal dysplasia and immunodeficiency 1 (EDAID1) | Ultra-Rare | — | 1 | |
| Ectodermal dysplasia and immunodeficiency 2 (EDAID2) | Very Rare | — | 1 | |
| Fanconi anemia complementation group T (FANCT) | Rare | — | 1 | |
| Granulomatous disease, chronic, autosomal recessive, 2 (CGD2) | Very Rare | — | 1 | |
| Immunodeficiency 100 with pulmonary alveolar proteinosis and hypogammaglobulinemia (IMD100) | Ultra-Rare | 5 | 1 | |
| Immunodeficiency 106, susceptibility to viral infections (IMD106) | N/A | — | 1 | |
| Immunodeficiency 107, susceptibility to invasive Staphylococcus aureus infection (IMD107) | N/A | — | 1 | |
| Immunodeficiency 109 with lymphoproliferation (IMD109) | Ultra-Rare | — | 1 | |
| Immunodeficiency 110 with lymphoproliferation (IMD110) | Ultra-Rare | — | 1 | |
| Immunodeficiency 116 (IMD116) | Ultra-Rare | 5 | 1 | |
| Immunodeficiency 127 (IMD127) | N/A | — | 1 | |
| Immunodeficiency 14A with lymphoproliferation, autosomal dominant (IMD14A) | N/A | 5 | 1 | |
| Immunodeficiency 14B, autosomal recessive (IMD14B) | Ultra-Rare | — | 1 | |
| Immunodeficiency 15A (IMD15A) | N/A | — | 1 | |
| Immunodeficiency 15B (IMD15B) | Ultra-Rare | — | 1 | |
| Immunodeficiency 22 (IMD22) | Ultra-Rare | — | 1 | |
| Immunodeficiency 29 (IMD29) | Ultra-Rare | 5 | 1 | |
| Immunodeficiency 33 (IMD33) | Very Rare | — | 1 | |
| Immunodeficiency 38, with basal ganglia calcification (IMD38) | Ultra-Rare | 5 | 1 | |
| Immunodeficiency 43 (IMD43) | Ultra-Rare | 5 | 1 | |
| Immunodeficiency 44 (IMD44) | Ultra-Rare | — | 1 | |
| Immunodeficiency 48 (IMD48) | N/A | — | 1 | |
| Immunodeficiency 50 (IMD50) | Ultra-Rare | — | 1 | |
| Immunodeficiency 53 (IMD53) | Ultra-Rare | — | 1 | |
| Immunodeficiency 57 with autoinflammation (IMD57) | Ultra-Rare | — | 1 | |
| Immunodeficiency 63 with lymphoproliferation and autoimmunity (IMD63) | N/A | 5 | 1 | |
| Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia (IMD73B) | Ultra-Rare | — | 1 | |
| Immunodeficiency 73C with defective neutrophil chemotaxis and hypogammaglobulinemia (IMD73C) | Ultra-Rare | — | 1 | |
| Immunodeficiency 82 with systemic inflammation (IMD82) | N/A | — | 1 | |
| Immunodeficiency 97 with autoinflammation (IMD97) | N/A | — | 1 | |
| Immunodeficiency due to defect in MAPBP-interacting protein (ID-MAPBPIP) | Ultra-Rare | — | 1 | |
| Infections, recurrent, associated with encephalopathy, hepatic dysfunction and cardiovascular malformations (IEHDCM) | Ultra-Rare | — | 1 | |
| Lymphoproliferative syndrome 1 (LPFS1) | Ultra-Rare | — | 1 | |
| Lymphoproliferative syndrome 3 (LPFS3) | Ultra-Rare | — | 1 | |
| Lymphoproliferative syndrome, X-linked, 1 (XLP1) | Ultra-Rare | 2 | 1 |