2026 ICD-10-CM Diagnosis Code G82.22Paraplegia, incomplete
ICD-10-CM Codes›G00–G99›G80-G83›paraparesis
- Billable — Valid for Submission
- Chronic Condition
G82.22 is a billable ICD-10-CM diagnosis code for paraplegia, incomplete. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026). Coders also document this condition as incomplete paraplegia. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Paralysis (other than cerebral palsy).
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Incomplete paraplegia
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- incomplete - G82.22
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Paraplegia(lower)
- incomplete
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Paraparesis, Tropical Spastic
a subacute paralytic myeloneuropathy occurring endemically in tropical areas such as the caribbean, colombia, india, and africa, as well as in the southwestern region of japan; associated with infection by human t-cell leukemia virus i. clinical manifestations include a slowly progressive spastic weakness of the legs, increased reflexes, babinski signs, incontinence, and loss of vibratory and position sensation. on pathologic examination inflammatory, demyelination, and necrotic lesions may be found in the spinal cord. (adams et al., principles of neurology, 6th ed, p1239)Paraplegia
severe or complete loss of motor function in the lower extremities and lower portions of the trunk. this condition is most often associated with spinal cord diseases, although brain diseases; peripheral nervous system diseases; neuromuscular diseases; and muscular diseases may also cause bilateral leg weakness.Spastic Paraplegia, Hereditary
a group of inherited diseases that share similar phenotypes but are genetically diverse. different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity. peripheral sensory neurons may be affected in the later stages of the disease. (j neurol neurosurg psychiatry 1998 jan;64(1):61-6; curr opin neurol 1997 aug;10(4):313-8)
Patient EducationClinical
Paralysis
Paralysis is the loss of muscle function in part of your body. It happens when something goes wrong with the way messages pass between your brain and muscles. Paralysis can be complete or partial. It can occur on one or both sides of your body. It can also occur in just one area, or it can be widespread.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert G82.22 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About G82.22Overview
Is G82.22 (Paraplegia) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report paraplegia, incomplete on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What is the ICD-9 equivalent of G82.22?
Under the General Equivalence Mappings, paraplegia, incomplete converts to ICD-9-CM 344.1 (paraplegia NOS). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
