FA38.3

ICD-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 disorders
  • FA24.2 – psoriatic and enteropathic arthropathies juvenile
  • FB0Y – neuropathic spondylopathy
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  • http://id.who.int/icd/entity/1989556002 – Conditions associated with the spine
  • 01 – Certain infectious or parasitic diseases
  • 05 – Endocrine, nutritional or metabolic diseases
  • 18 – Complications of pregnancy, childbirth and the puerperium
  • 19 – Certain conditions originating in the perinatal period
  • 22 – Injury, poisoning or certain other consequences of external causes
  • DA0E.8 – Temporomandibular joint disorders

Sibling codes

  • FA38.0 – Diabetic arthropathy
  • FA38.1 – Neuropathic arthropathy
  • FA38.2 – Arthropathy in hypersensitivity reactions classified elsewhere
  • FA38.Y – Arthropathy in other specified diseases classified elsewhere

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