FA38.3ICD-11 MMS 2026-01
Haemophilic arthropathy
Description
Joint destruction in the knees, shoulders, ankles, elbows, and hips is associated with haemophilia. The condition includes acute hemarthrosis, subacute or chronic arthritis, and end-stage haemophilic arthropathy. Nearly all patients with severe haemophilia A or B and half of patients with moderate disease activity experience hemarthrosis. Symptoms include joint pain, joint swelling, joint fibrosis, development of flexion deformities, and erosion of joint cartilage. Joints most commonly affected are knees, ankles, elbows, shoulders, and hips (in order of frequency). Bleeding into muscle and soft tissue also causes musculoskeletal dysfunction.
Index terms
- Haemophilic arthropathy
Exclusions from above levels
03– arthropathy in: haematological disordersFA24.2– psoriatic and enteropathic arthropathies juvenileFB0Y– neuropathic spondylopathy
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- http://id.who.int/icd/entity/1989556002 – Conditions associated with the spine
01– Certain infectious or parasitic diseases05– Endocrine, nutritional or metabolic diseases18– Complications of pregnancy, childbirth and the puerperium19– Certain conditions originating in the perinatal period22– Injury, poisoning or certain other consequences of external causesDA0E.8– Temporomandibular joint disorders
Sibling codes
Foundation entity
Haemophilic arthropathy – http://id.who.int/icd/entity/1660841611
Allowed postcoordination axes
Part of: FA38: Arthropathy in diseases classified elsewhere › 15: Diseases of the musculoskeletal system or connective tissue