ICD10 code of Charcot-Marie-Tooth Disease and ICD9 code
What is the ICD10 code for Charcot-Marie-Tooth Disease? And the ICD9 code for Charcot-Marie-Tooth Disease?
Charcot-Marie-Tooth Disease (CMT) is a hereditary neurological disorder that affects the peripheral nerves, leading to muscle weakness and sensory loss. It is named after the three physicians who first described the condition: Jean-Martin Charcot, Pierre Marie, and Howard Henry Tooth. CMT is characterized by progressive muscle wasting and weakness, especially in the lower limbs, resulting in difficulties with walking, balance, and coordination.
In the International Classification of Diseases, 10th Revision (ICD-10), Charcot-Marie-Tooth Disease is classified under the code G60.0. This code specifically refers to CMT and includes all its subtypes, such as CMT1, CMT2, and CMTX. The ICD-10 code G60.0 allows healthcare providers and researchers to accurately identify and track cases of CMT for statistical and diagnostic purposes.
In the previous version of the classification system, the International Classification of Diseases, 9th Revision (ICD-9), Charcot-Marie-Tooth Disease was classified under the code 356.1. This code encompassed various hereditary and idiopathic peripheral neuropathies, including CMT.
It is important to note that ICD codes are used primarily for billing, medical records, and statistical purposes. They provide a standardized way of classifying and documenting diseases, allowing for accurate data analysis and comparison across healthcare systems. However, they do not provide detailed clinical information about the disease or its management.
In conclusion, the ICD-10 code for Charcot-Marie-Tooth Disease is G60.0, while the corresponding ICD-9 code is 356.1. These codes enable healthcare professionals and researchers to classify and track cases of CMT, aiding in accurate diagnosis and appropriate management of this neurological disorder.
by Diseasemaps
CMT 1A, And many more
5/21/18 by Joe 4050
They are different genetic markers of CMT.
5/22/18 by Dawn 4050
356.1 for Charcot-Marie-Tooth
CMT has a ICD10 code. It is a disease of the nervous system. This really applies to people who have CMT type 1 2 3 and 4
DON'T KNOW IF THIS HELPS, BUT...
Charcot-Marie-Tooth Disease
Atrophy, Muscular, Peroneal | HMSN Type I | HMSN Type II | Hereditary Motor and Sensory-Neuropathy Type II | Hereditary Motor, and Sensory Neuropathy Type I | Muscular Atrophy, Peroneal | Peroneal Muscular Atrophy | Roussy-Levy Syndrome
A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343)
5/29/18 by Daniel 4200
These are diagnosis and billing codes used for insurance purposes
2/7/20 by Roberta 1900
https://www.icd10data.com/ICD10CM/Codes/G00-G99/G60-G65/G60-/G60.0
2/8/20 by Angela 100
I DO NOT KNOW THOSE CODES.
2/9/20 by Jim 3000
Manifest the degree of the disease
9/4/17 by Lorena. Translated
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