A type 1 interferonopathy that occurs during childhood.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Aicardi-Goutieres syndrome | MONDO:0018866 | 11 | |
| Proteosome-associated autoinflammatory syndrome | MONDO:0009726 | 6 | |
| Singleton-Merten dysplasia | MONDO:0008429 | 2 | |
| Autoimmune interstitial lung disease-arthritis syndrome | MONDO:0014629 | 2 | |
| Familial chilblain lupus | MONDO:0018827 | 2 | |
| Trichohepatoenteric syndrome | MONDO:0009105 | 2 | |
| STING-associated vasculopathy with onset in infancy | MONDO:0014405 | STING1 | |
| Spondyloenchondrodysplasia with immune dysregulation | MONDO:0011939 | ACP5 | |
| X-linked reticulate pigmentary disorder | MONDO:0010523 | POLA1 | |
| Deficiency of adenosine deaminase 2 | MONDO:0014306 | ADA2 | |
| Pseudo-TORCH syndrome 2 | MONDO:0018828 | USP18 | |
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | MONDO:0008641 |
Rare disease
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