Incoming and outgoing links Monogenic Autoinflammatory diseases and skin
Back to articleIncoming links
- Adult onset still disease
- AiKDs
- Familial cold inflammatory syndrome 1
- Mutation
- MVK gene
- NLRP12-associated systemic autoinflammatory disease
- Nod-like receptors
- Papa syndrome
- Sapho syndrome
- Schnitzler syndrome
- Spondyloenchondrodysplasia
- Sting-associated vasculopathy
- STING-associated vasculopathy with onset in infancy
- Systemic juvenile idiopathic arthritis (Still syndrome)
- Yao-syndrome
Outgoing links
- ADAM17 deficiency
- Adenosine deaminase deficiency
- Aicardi-goutières syndrome
- AiKDs
- Ap1s3 gene
- Autoinflammatory Periodic Fever, Immunodeficiency, and Thrombocytopenia
- Autoinflammatory Syndrome, Familial, Behcet-Like
- Blue syndrome
- Candle syndrome
- CARD14 – Associated Papulosquamous Eruption
- C/EBPepsilon-Associated Autoinflammation and Immune Impairment of Neutrophils
- Cryopyrin-associated periodic syndrome
- Deficiency of IL-1 Receptor Antagonist
- Deficiency of IL-36 receptor antagonist
- Familial Chilblain Lupus
- Familial cold autoinflammatory syndrome 3
- Familial cold autoinflammatory syndrome 4
- Familial cold-induced autoinflammatory syndrome 2
- Familial cold inflammatory syndrome 1
- Familial mediterranean fever
- Fever syndromes, hereditary, periodic (overview)
- HOIL-1 Deficiency
- H syndrome
- Hyper IgD syndrome
- Majeed syndrome
- MEFV Gene
- Muckle-wells syndrome
- NFKB1-Associated Autoinflammatory Diseases
- NLRP12-associated systemic autoinflammatory disease
- NLRP1-associated autoinflammation with arthritis and dyskeratosis
- Otulin-Related Autoinflammatory Syndrome
- Papa syndrome
- PID autoinflammatory diseases
- Proteasome-associated autoinflammatory syndrome 2
- Pyrin-associated autoinflammation with neutrophilic dermatosis
- RELA Haploinsufficiency
- Singleton-merten syndrome
- Sting-associated vasculopathy
- Toll-like receptor 8
- Tumor necrosis factor receptor associated periodic syndrome
- Urticaria vibratory