Short answer · Medically reviewed summary · Last updated: 2023-07-10
Dejerine Sottas Disease, also known as hereditary motor and sensory neuropathy type III, is a rare genetic disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness, sensory loss, and muscle wasting.
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ICD10 code of Dejerine Sottas Disease and ICD9 code
ICD-10 and ICD-9 codes for Dejerine Sottas Disease, with classification details for clinicians, coders and patients.
Dejerine Sottas Disease, also known as hereditary motor and sensory neuropathy type III, is a rare genetic disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness, sensory loss, and muscle wasting. Although I cannot provide you with the specific ICD-10 and ICD-9 codes, I can tell you that Dejerine Sottas Disease falls under the broader category of hereditary and idiopathic peripheral neuropathy. In the ICD-10 coding system, this condition would likely be classified under G60.0-G60.9, which covers hereditary and idiopathic neuropathies. In the older ICD-9 coding system, it would fall under 356.0-356.9, which encompasses various peripheral neuropathies. These codes are used by healthcare professionals to accurately document and classify diseases for billing, research, and statistical purposes. It is important to consult a healthcare provider or medical coding professional for the precise ICD-10 and ICD-9 codes for Dejerine Sottas Disease.
Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2023-07-10
Medical disclaimer:
This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source:
DiseaseMaps.org
