FA23ICD-11 MMS 2026-01
Adult-onset Still disease
Description
Adult onset Still's disease is a rare rheumatic condition characterised by a combination of symptoms, such as fever higher than 39 degrees C, cutaneous rash during fever peaks, joint or muscle pain, lymph node hypertrophy, increase of white blood cells (especially polymorphonuclear neutrophils) and abnormalities of liver metabolism.
Index terms
- Adult-onset Still disease
- Adult-onset Still disease, multiple sites
- Adult-onset Still disease, shoulder region
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- Adult-onset Still disease, acromioclavicular joint
- Adult-onset Still disease, glenohumeral joint
- Adult-onset Still disease, sternoclavicular joint
- Adult-onset Still disease, upper arm
- Adult-onset Still disease, elbow joint
- Adult-onset Still disease, forearm
- Adult-onset Still disease, wrist joint
- Adult-onset Still disease, hand
- Adult-onset Still disease, carpus
- Adult-onset Still disease, fingers
- Adult-onset Still disease, metacarpus
- Adult-onset Still disease, pelvic region or thigh
- Adult-onset Still disease, buttock
- Adult-onset Still disease, hip joint
- Adult-onset Still disease, lower leg
- Adult-onset Still disease, knee joint
- Adult-onset Still disease, ankle or foot
- Adult-onset Still disease, metatarsus
- Adult-onset Still disease, tarsus
- Adult-onset Still disease, toes
- Adult-onset Still disease, ankle joint
- Adult-onset Still disease, other joints in foot
- Adult-onset Still disease, head
- Adult-onset Still disease, neck
- Adult-onset Still disease, vertebral column
- Erosive Adult-onset Still disease
- Non-erosive Adult-onset Still disease
Excludes
FA24.4– Still disease NOS
Exclusions from above levels
Sibling codes
Foundation entity
Adult-onset Still disease – http://id.who.int/icd/entity/549009522
Allowed postcoordination axes
Part of: 15: Diseases of the musculoskeletal system or connective tissue