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ICD10 code of Human HOXA1 Syndromes and ICD9 code

What is the ICD10 code for Human HOXA1 Syndromes? And the ICD9 code for Human HOXA1 Syndromes?

ICD9 and ICD10 codes of Human HOXA1 Syndromes

The ICD-10 code for Human HOXA1 Syndromes is Q87.8. This code is used to classify and identify specific genetic disorders related to the HOXA1 gene. Unfortunately, there is no specific ICD-9 code for this syndrome as ICD-9 does not have a direct equivalent for Q87.8. It is important to consult with a healthcare professional for accurate diagnosis and coding information.
Human HOXA1 Syndromes, also known as Bosley-Salih-Alorainy syndrome, is a rare genetic disorder that affects multiple systems in the body. It is characterized by a variety of symptoms including facial paralysis, hearing loss, and defects in the development of the inner ear, eyes, and teeth. The condition is caused by mutations in the HOXA1 gene.

As for the ICD10 code, the specific code for Human HOXA1 Syndromes is Q87.0. The ICD10 coding system is used worldwide to classify diseases and medical conditions for billing and statistical purposes. This code allows healthcare professionals to accurately document and track cases of this particular syndrome.

Regarding the ICD9 code, it is important to note that the ICD9 coding system has been replaced by ICD10 since October 1, 2015. Prior to this transition, the ICD9 code for Human HOXA1 Syndromes was 756.0. However, it is crucial to utilize the current ICD10 code for accurate and up-to-date medical coding.

It is important to consult with a healthcare professional or medical coder for the most accurate and comprehensive information on ICD10 codes and their corresponding conditions.
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ICD9 and ICD10 codes of Human HOXA1 Syndromes

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World map of Human HOXA1 Syndromes

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