Short answer · Medically reviewed summary · Last updated: 2023-07-10
Shprintzen-Goldberg Syndrome (SGS), also known as velo-cardio-facial syndrome or 22q11.2 deletion syndrome, is a rare genetic disorder characterized by a combination of craniofacial, cardiovascular, and neurodevelopmental anomalies. The International Classification of Diseases, Tenth Revision (ICD-10) provides a specific code to identify this condition. The ICD-10 code for Shprintzen-Goldberg Syndrome is Q87.1.
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ICD10 code of Shprintzen-Goldberg Syndrome and ICD9 code
ICD-10 and ICD-9 codes for Shprintzen-Goldberg Syndrome, with classification details for clinicians, coders and patients.
Shprintzen-Goldberg Syndrome (SGS), also known as velo-cardio-facial syndrome or 22q11.2 deletion syndrome, is a rare genetic disorder characterized by a combination of craniofacial, cardiovascular, and neurodevelopmental anomalies. The International Classification of Diseases, Tenth Revision (ICD-10) provides a specific code to identify this condition.
The ICD-10 code for Shprintzen-Goldberg Syndrome is Q87.1. This alphanumeric code falls under the category of "Congenital malformation syndromes predominantly associated with short stature" (Q87). The fourth character "1" denotes Shprintzen-Goldberg Syndrome specifically.
In contrast, the ICD-9 code system, which was used prior to the implementation of ICD-10, assigned a different code for this syndrome. The ICD-9 code for Shprintzen-Goldberg Syndrome was 758.32. It was classified under the section "Other anomalies of the face and neck" (ICD-9 code range 744-748).
It is important to note that the transition from ICD-9 to ICD-10 occurred on October 1, 2015, so healthcare providers and medical coders have been using ICD-10 codes for several years now. The updated coding system allows for more precise identification and classification of diseases and disorders, aiding in accurate medical record keeping, research, and healthcare management.
In summary, the ICD-10 code for Shprintzen-Goldberg Syndrome is Q87.1, while the previous ICD-9 code was 758.32. These codes are utilized to categorize and track specific conditions, enabling healthcare professionals to accurately diagnose and manage patients with this rare genetic disorder.
The ICD-10 code for Shprintzen-Goldberg Syndrome is Q87.1. This alphanumeric code falls under the category of "Congenital malformation syndromes predominantly associated with short stature" (Q87). The fourth character "1" denotes Shprintzen-Goldberg Syndrome specifically.
In contrast, the ICD-9 code system, which was used prior to the implementation of ICD-10, assigned a different code for this syndrome. The ICD-9 code for Shprintzen-Goldberg Syndrome was 758.32. It was classified under the section "Other anomalies of the face and neck" (ICD-9 code range 744-748).
It is important to note that the transition from ICD-9 to ICD-10 occurred on October 1, 2015, so healthcare providers and medical coders have been using ICD-10 codes for several years now. The updated coding system allows for more precise identification and classification of diseases and disorders, aiding in accurate medical record keeping, research, and healthcare management.
In summary, the ICD-10 code for Shprintzen-Goldberg Syndrome is Q87.1, while the previous ICD-9 code was 758.32. These codes are utilized to categorize and track specific conditions, enabling healthcare professionals to accurately diagnose and manage patients with this rare genetic disorder.
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
