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17 relations: Anakinra, Canakinumab, Cold urticaria, Cryopyrin-associated periodic syndrome, Deficiency of the interleukin-1–receptor antagonist, List of cutaneous conditions, List of diseases (C), List of syndromes, Muckle–Wells syndrome, NALP3, NLRC4, PAPA syndrome, Periodic fever syndrome, Primary immunodeficiency, Pyroptosis, Rilonacept, Schnitzler syndrome.
Anakinra
Anakinra (brand name Kineret) is a biopharmaceutical drug used to treat rheumatoid arthritis.
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Canakinumab
Canakinumab (INN, trade name Ilaris, previously ACZ885) is a human monoclonal antibody targeted at interleukin-1 beta.
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Cold urticaria
Cold urticaria (essentially meaning "cold hives") is a disorder where hives (urticaria) or large red welts form on the skin after exposure to a cold stimulus.
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Cryopyrin-associated periodic syndrome
Cryopyrin-associated periodic syndrome (CAPS) is a group of rare, heterogeneous autoinflammatory disease characterized by interleukin 1β-mediated systemic inflammation and clinical symptoms involving skin, joints, central nervous system, and eyes.
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Deficiency of the interleukin-1–receptor antagonist
Deficiency of the interleukin-1–receptor antagonist (DIRA) is a autosomal recessive, genetic autoinflammatory syndrome resulting from mutations in IL1RN, the gene encoding the interleukin 1 receptor antagonist.
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List of cutaneous conditions
Many conditions affect the human integumentary system—the organ system covering the entire surface of the body and composed of skin, hair, nails, and related muscle and glands.
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List of diseases (C)
This is a list of diseases starting with the letter "C".
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List of syndromes
This is an alphabetically-sorted list of medical syndromes.
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Muckle–Wells syndrome
Muckle–Wells syndrome (MWS), also known as urticaria-deafness-amyloidosis syndrome (UDA), is a rare autosomal dominant disease which causes sensorineural deafness and recurrent hives, and can lead to amyloidosis.
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NALP3
NACHT, LRR and PYD domains-containing protein 3 (NALP3), also known as cryopyrin, is a protein that in humans is encoded by the NLRP3 gene located on the long arm of chromosome 1.
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NLRC4
NLR family CARD domain-containing protein 4 is a protein that in humans is encoded by the NLRC4 gene.
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PAPA syndrome
PAPA syndrome is an acronym for pyogenic arthritis, pyoderma gangrenosum and acne.
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Periodic fever syndrome
Periodic fever syndromes (also known as autoinflammatory diseases or autoinflammatory syndromes) are a set of disorders characterized by recurrent episodes of systemic and organ-specific inflammation.
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Primary immunodeficiency
Primary immunodeficiencies are disorders in which part of the body's immune system is missing or does not function normally.
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Pyroptosis
Pyroptosis is a highly inflammatory form of programmed cell death that occurs most frequently upon infection with intracellular pathogens and is likely to form part of the antimicrobial response.
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Rilonacept
Rilonacept, also known as IL-1 Trap (marketed by Regeneron Pharmaceuticals under the trade name Arcalyst), is an interleukin 1 inhibitor.
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Schnitzler syndrome
Schnitzler syndrome is a rare disease characterised by onset around middle age of chronic hives (urticaria) and periodic fever, bone pain and joint pain (sometimes with joint inflammation), weight loss, malaise, fatigue, swollen lymph glands and enlarged spleen and liver.
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Redirects here:
Ansell-Bywaters-Elderking syndrome, CINCA, Chronic Neurologic Cutaneous and Articular Syndrome, Chronic infantile neurologic cutaneous and articular syndrome, Chronic, infantile, neurological, cutaneous, articular syndrome, NOMID, Neonatal onset multisystem inflammatory disease, Prieur Griscelli syndrome, Prieur-Griscelli syndrome.
References
[1] https://en.wikipedia.org/wiki/Neonatal-onset_multisystem_inflammatory_disease
