Incoming and outgoing links PID autoinflammatory diseases
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- ACP5 Gene
- Acute generalized exanthematous pustulosis
- ADA2 Gene
- ADAM17gene
- ADAR Gene
- Adenosine Deaminase 2 Deficiency
- Aicardi-goutières syndrome
- ALPI Gene
- Ap1s3 gene
- Atrophoderma vermiculatum
- Autoinflammatory Syndrome, Familial, Behcet-Like
- Autoinflammatory syndrome, familial, X-linked, Behcet-like
- BCL10 Gene
- Blue syndrome
- Candle syndrome
- CARD14 Gene
- Caspasen
- Chilblain lupus
- Chronic infantile neurological cutaneous and articular syndrome
- Chronic recurrent multifocal osteomyelitis
- Cutaneous amyloidosis (overview)
- Deficiency of IL-1 Receptor Antagonist
- Dermatomyositis (overview)
- DNASE1L3 Gene
- DNASE2 Gene
- Dyschromatosis symmetrica hereditaria
- ELF4 Gene
- Familial cold autoinflammatory syndrome 3
- Familial cold autoinflammatory syndrome 4
- Familial cold-induced autoinflammatory syndrome 2
- Familial cold inflammatory syndrome 1
- Familial cold urticaria
- Familial mediterranean fever
- Hairy cell leukemia
- HAVCR2 Gene
- H syndrome
- Hyper-IgD syndrome
- IFIH1 Gene
- IL1RN Gene
- Immunodeficiency 100 with pulmonary alveolar proteinosis and hypogammaglobulinemia
- Inflammasome
- Interleukin 1 family
- Interleukin 36 receptor antagonist
- LPIN2 Gene
- Lupus erythematosus systemic
- Majeed syndrome
- Malaria
- MEFV Gene
- Mevalonic aciduria
- Muckle-wells syndrome
- MVK gene
- NLRC4 Gene
- NLRP1
- NLRP12 Gene
- NLRP3 Gene
- NLRP3 protein
- Nod2
- NOMID
- OAS1-gene
- OTULIN Gene
- Otulin-Related Autoinflammatory Syndrome
- Papa syndrome
- PLCG2 Gene
- POLA1 Gene
- Proteasome
- PSMA3 Gene
- PSMB8 Gene
- Psoriasis pustulosa
- PSTPIP1 Gene
- Pulmonary alveolar proteinosis
- Pustular psoriasis
- Pustulosis palmaris et plantaris
- Pyoderma gangraenosum
- Pyrin
- Regional enteritis
- Respiratory papillomatosis, juvenile recurrent, congenital
- RNASEH2A Gene
- RNASEH2B Gene
- RNASEH2C Gene
- Rosai-Dorfman-Syndrom
- Samhd1 GEne
- SLC29A3 Gene
- Sneddon syndrome
- STING1-gene
- Subcutaneous panniculitis-like t-cell lymphoma
- Suppurative hidradenitis
- Sweet syndrome
- TNFAIP3 Gene
- Tnf-receptor associated periodic fever
- TNFRSF1A Gene
- Trex1 gene
- Urticaria vasculitis
- X-linked reticulate pigmentary disorder with systemic manifestations