Idiopathic rhabdomyolysis

Description

Skeletal muscle breakdown with leakage of muscle contents, frequently accompanied by myoglobinuria, occurring in both adult and paediatric populations with no identifiable cause. The attacks are often recurrent. Renal failure due to tubular necrosis is a severe complication.

Index terms

Idiopathic rhabdomyolysis
rhabdomyolysis NOS

Excludes

http://id.who.int/icd/entity/1159616108 – Secondary myopathies
http://id.who.int/icd/entity/1425591047 – Myasthenia gravis or certain specified neuromuscular junction disorders

Exclusions from above levels

NF0A.6 – Volkmann ischaemic contracture
8D44.1 – Alcoholic myopathy
8E4A.0 – Stiff person syndrome

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FB56.2 – Myalgia
http://id.who.int/icd/entity/833816211 – Primary disorders of muscles
MB47.3 – Cramp or spasm
8C70 – Muscular dystrophy
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

FB32.2Y – Other specified ischaemic infarction of muscle
FB32.2Z – Ischaemic infarction of muscle, unspecified

Foundation entity

Idiopathic rhabdomyolysis – http://id.who.int/icd/entity/2029533852

Allowed postcoordination axes

Part of: FB32.2: Ischaemic infarction of muscle › FB32: Certain specified disorders of muscle › 15: Diseases of the musculoskeletal system or connective tissue