Verweise von und zu Monogenic Autoinflammatory diseases and skin
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- AiKDs
- Familial cold inflammatory syndrome 1
- Mutation
- MVK gene
- NLRP12-associated systemic autoinflammatory disease
- Nod-like receptors
- Papa syndrome
- Sapho syndrome
- Schnitzler syndrome
- Spondyloenchondrodysplasia
- Adult onset still disease
- STING-associated vasculopathy with onset in infancy
- Sting-associated vasculopathy
- Systemic juvenile idiopathic arthritis (Still syndrome)
- Yao-syndrome
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- ADAM17 deficiency
- Adenosine deaminase deficiency
- Aicardi-goutières syndrome
- AiKDs
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- Otulin-Related Autoinflammatory Syndrome
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- Autoinflammatory Syndrome, Familial, Behcet-Like
- Blue syndrome
- Candle syndrome
- CARD14 – Associated Papulosquamous Eruption
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- Familial Chilblain Lupus
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- H syndrome
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- Deficiency of IL-1 Receptor Antagonist
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- Familial cold inflammatory syndrome 1
- Familial cold-induced autoinflammatory syndrome 2
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- Majeed syndrome
- MEFV Gene
- Muckle-wells syndrome
- NFKB1-Associated Autoinflammatory Diseases
- NLRP12-associated systemic autoinflammatory disease
- NLRP1-associated autoinflammation with arthritis and dyskeratosis
- Papa syndrome
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- Pyrin-associated autoinflammation with neutrophilic dermatosis
- RELA Haploinsufficiency
- Singleton-merten syndrome
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