FA27.0ICD-11 MMS 2026-01
Kashin-Beck disease
Description
Kashin-Beck disease (KBD) is a chronic, endemic osteochondropathy of unknown etiology. The disease is mainly distributed in a diagonal belt ranging from the northeast to the southwest of China, where the soil selenium content is low. Mineral deficiencies (e.g., selenium, iodine), fungal cereal contamination, and water contamination may be contributing factors to its etiology. The disease is manifested by arthritic pain, morning stiffness, enlarged and shortened fingers, deformed and enlarged joints, and limited motion of the joints in the extremities.
Index terms
- Kashin-Beck disease
- Kaschin-Beck disease
- Kaschin-Beck disease, unspecified site
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- Kashin-Bek disease
- Urov disease
- Kaschin-Beck disease, multiple sites
- Kaschin-Beck disease, shoulder region
- Kaschin-Beck disease, acromioclavicular joint
- Kaschin-Beck disease, clavicle
- Kaschin-Beck disease, glenohumeral joint
- Kaschin-Beck disease, sternoclavicular joint
- Kaschin-Beck disease, upper arm
- Kaschin-Beck disease, elbow joint
- Kaschin-Beck disease, forearm
- Kaschin-Beck disease, wrist joint
- Kaschin-Beck disease, hand
- Kaschin-Beck disease, carpus
- Kaschin-Beck disease, fingers
- Kaschin-Beck disease, metacarpus
- Kaschin-Beck disease, pelvic region or thigh
- Kaschin-Beck disease, buttock
- Kaschin-Beck disease, hip joint
- Kaschin-Beck disease, lower leg
- Kaschin-Beck disease, knee joint
- Kaschin-Beck disease, ankle or foot
- Kaschin-Beck disease, metatarsus
- Kaschin-Beck disease, tarsus
- Kaschin-Beck disease, toes
- Kaschin-Beck disease, ankle joint
- Kaschin-Beck disease, other joints in foot
- Kashin-Beck disease, head
- Kashin-Beck disease, neck
- Kashin-Beck disease, vertebral column
Exclusions from above levels
Sibling codes
Foundation entity
Kashin-Beck disease – http://id.who.int/icd/entity/211396970
Allowed postcoordination axes
Part of: FA27: Certain specified inflammatory arthropathies › 15: Diseases of the musculoskeletal system or connective tissue