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2025 ICD-10-CM code M36

Systemic disorders of connective tissue in diseases classified elsewhere.

Refer to the official ICD-10-CM coding guidelines for complete and accurate coding practices.Ensure that all relevant codes are used to capture the patient's condition fully.Consider using additional codes to represent organ-specific manifestations.

Modifiers are not applicable to ICD-10 codes.

Medical necessity for services related to M36 is established through comprehensive clinical documentation supporting the presence of a systemic connective tissue disorder.The severity and extent of symptoms, the need for diagnostic testing and therapies, and the overall impact on the patient's health must be clearly documented to justify medical necessity.Refer to payer-specific guidelines for additional requirements.

The clinical responsibility for patients with M36 involves a multidisciplinary approach.A rheumatologist usually leads the care, coordinating with other specialists (e.g., cardiologist, pulmonologist, nephrologist) as needed based on the specific organ involvement.The physician's duties include taking a detailed history, performing a thorough physical examination, ordering and interpreting diagnostic tests (including imaging and laboratory studies), and developing a comprehensive treatment plan (including medication management, physical therapy referrals, and monitoring for complications).

IMPORTANT:This code is used when the specific connective tissue disorder is classified elsewhere.Consider codes for specific conditions such as Systemic Lupus Erythematosus (SLE), Rheumatoid Arthritis (RA), Scleroderma, Polymyositis/Dermatomyositis, and Mixed Connective Tissue Disease (MCTD), among others.Always refer to the complete ICD-10-CM manual for the most accurate coding.

In simple words: This code is for a problem affecting multiple parts of the body because of a problem with the body's connective tissues (tissues that hold things together).It's used when the specific type of problem is already coded elsewhere.Symptoms can include tiredness, fever, joint and muscle pain, weakness, trouble swallowing, and shortness of breath. Doctors use a combination of physical exams, tests, and images to make a diagnosis and might prescribe medication or physical therapy.

M36, Systemic disorders of connective tissue in diseases classified elsewhere, encompasses systemic disorders affecting multiple organs due to abnormal immune responses within connective tissues.This code is applied when the specific connective tissue disorder is classified elsewhere in the ICD-10-CM coding system.The condition involves tissues that connect, support, bind, or separate, leading to symptoms like fatigue, fever, joint and muscle pain, weakness, dysphagia, and dyspnea. Diagnosis relies on patient history, physical examination, imaging (e.g., X-rays), and lab tests (antibodies, enzyme levels). Treatment may include exercise therapy, corticosteroids, immunosuppressants, and antirheumatic medications.

Example 1: A 45-year-old female presents with fatigue, joint pain, and Raynaud's phenomenon.Initial laboratory tests reveal positive antinuclear antibodies (ANA) and elevated inflammatory markers.Further workup suggests a systemic connective tissue disorder, and the provider documents features suggestive of both lupus and scleroderma. However, the patient does not meet the full diagnostic criteria for either condition.In this scenario, M36 would be used, pending further evaluation and clarification of the precise diagnosis.The patient's specific organ system involvement should be coded separately, if appropriate., A 60-year-old male presents with generalized weakness, difficulty swallowing, and shortness of breath.Physical examination reveals myositis and skin changes consistent with dermatomyositis.However, the patient's symptoms are far more widespread than what typically defines this condition. Blood tests show positive ANA and elevated muscle enzymes. In this case, M36 is used pending a comprehensive evaluation of his disease, to reflect the systemic involvement.The provider documents the dermatomyositis separately with its own ICD-10 code, because it is a significant part of the clinical picture., A 30-year-old female presents with fever, fatigue, and joint pain.Extensive laboratory tests reveal positive ANA and anti-dsDNA antibodies and other evidence of systemic lupus erythematosus. The physician diagnoses lupus nephritis (coded separately), along with other systemic manifestations of the disease. In this case, although SLE is coded specifically, M36 might be considered as a secondary code if there is a broader range of system-wide abnormalities not fully captured by SLE specific codes to completely reflect the patient's condition.

Detailed patient history, including onset, duration, and progression of symptoms.Complete physical examination findings.Results of all relevant laboratory tests (e.g., complete blood count, inflammatory markers, ANA, anti-dsDNA, other autoantibodies, enzyme levels).Imaging studies (e.g., X-rays, CT scans, MRI) as indicated.Documentation of any organ-specific manifestations requiring additional codes.Notes on treatment plan, including medications, therapies, and patient response.Note of any other diagnoses, to ensure they are appropriately coded.

** M36 is a residual category for systemic connective tissue disorders that do not fit into other more specific categories within the ICD-10-CM classification system.Always strive for the most specific code possible.If there is uncertainty about the precise diagnosis, additional clinical information and diagnostic studies should be sought before finalizing coding.

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