M32.9
Applicable To
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SLE NOS
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Systemic lupus erythematosus NOS
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Systemic lupus erythematosus without organ involvement
Approximate Synonyms
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Systemic lupus erythematosus
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Systemic lupus erythematosus sle)
Clinical Information
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A chronic inflammatory connective tissue disease marked by skin rashes, joint pain and swelling, inflammation of the kidneys, inflammation of the fibrous tissue surrounding the heart i.e., the pericardium), as well as other problems. Not all affected individuals display all of these problems.
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A chronic, inflammatory, connective tissue disease that can affect many organs including the joints, skin, heart, lungs, kidneys, and nervous system. It is marked by many different symptoms; however, not everyone with sle has all of the symptoms.
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A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of le cells in the blood or bone marrow.
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Chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes; it is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system; the disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of le cells in the blood or bone marrow.
Details
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M32.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
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The 2023 edition of ICD-10-CM M32.9 became effective on October 1, 2022.
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This is the American ICD-10-CM version of M32.9 – other international versions of ICD-10 M32.9 may differ.