Deficiency of the interleukin-1–receptor antagonist
autoinflammatory disease caused by mutations in the IL1RN gene, which encodes the IL1 receptor antagonist. It presents in infancy, and is characterized by systemic inflammation, pustular rash, bone pain, sterile osteitis, and periostitis
Press Enter · cited answer in seconds
0 sources
Deficiency of the interleukin-1–receptor antagonist
Summary
Deficiency of the interleukin-1–receptor antagonist is a class of disease[1].
Key Facts
- Deficiency of the interleukin-1–receptor antagonist's instance of is recorded as class of disease[2].
- Deficiency of the interleukin-1–receptor antagonist is a type of periodic fever syndrome[3].
- Deficiency of the interleukin-1–receptor antagonist is a type of autoinflammatory syndrome with immune deficiency[4].
- Deficiency of the interleukin-1–receptor antagonist is a type of autoinflammatory syndrome with skin involvement[5].
- Deficiency of the interleukin-1–receptor antagonist is a type of pyogenic autoinflammatory syndrome[6].
- Deficiency of the interleukin-1–receptor antagonist's NCI Thesaurus ID is recorded as C119056[7].
- Deficiency of the interleukin-1–receptor antagonist's health specialty is recorded as immunology[8].
- Deficiency of the interleukin-1–receptor antagonist's genetic association is recorded as IL1RN[9].
- Deficiency of the interleukin-1–receptor antagonist's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_210115[10].