Registrations in the EBMT Registry for autologous HSCT in autoimmune diseases (n=2515), June 2018*
| Multiple sclerosis | 1228 |
| Connective tissue | 699 |
| Systemic sclerosis | 540 |
| SLE | 108 |
| Polymyositis-dermatomyositis | 17 |
| Sjogren's syndrome | 4 |
| Antiphospholipid syndrome | 6 |
| Other/unknown | 24 |
| Arthritis | 166 |
| Rheumatoid arthritis | 80 |
| Juvenile chronic arthritis: | |
| Systemic JIA | 46 |
| Other JIA | 18 |
| Polyarticular JIA | 12 |
| Psoriatic arthritis | 3 |
| Other | 7 |
| Inflammatory bowel disease | 190 |
| Crohn's disease | 171 |
| Ulcerative colitis | 2 |
| Other | 17 |
| Haematological | 51 |
| Immune thrombocytopenia | 27 |
| Evans’ syndrome | 8 |
| Autoimmune haemolytic anaemia | 12 |
| Other | 4 |
| Vasculitis | 45 |
| Wegener's type | 10 |
| Behcet's disease | 9 |
| Takayasu | 2 |
| Polyarteritis | 3 |
| Churg-Strauss | 2 |
| HUVSOther/unknown | 118 |
| Other neurological | 98 |
| Neuromyelitis optica | 18 |
| CIDP | 47 |
| Myasthenia gravis | 8 |
| Other/unknown | 24 |
| Type 1 diabetes | 20 |
| Other/unknown | 18 |
*EBMT registry accessed 4 June 2018.
CIDP = Chronic inflammatory demyelinating polyneuropathy ; HUVS = hypocomplementemic urticarial vasculitis syndrome; JIA = juvenile idiopathic arthritis