Short answer · Medically reviewed summary · Last updated: 2023-07-10
Hallermann-Streiff syndrome (HSS) is a rare genetic disorder characterized by distinctive facial features and multiple systemic abnormalities. Although it is a well-defined syndrome, it does not have a specific ICD-10 code dedicated solely to it.
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ICD10 code of Hallermann Streiff Syndrome and ICD9 code
ICD-10 and ICD-9 codes for Hallermann Streiff Syndrome, with classification details for clinicians, coders and patients.
Hallermann-Streiff syndrome (HSS) is a rare genetic disorder characterized by distinctive facial features and multiple systemic abnormalities. Although it is a well-defined syndrome, it does not have a specific ICD-10 code dedicated solely to it. However, certain features of HSS can be coded individually using appropriate ICD-10 codes.
The most notable facial features of HSS include a small jaw, beaked nose, sunken eyes, and a thin bird-like appearance. These can be coded using specific facial anomaly codes such as Q18.1 for micrognathia (small jaw), Q30.0 for congenital malformation of the nose, and Q10.2 for microphthalmos (abnormally small eyes).
HSS is also associated with various systemic abnormalities. For instance, individuals with HSS often have skeletal abnormalities like a shortened stature or limb deformities. These can be coded using codes from the Q65-Q79 range, which cover congenital deformities of the musculoskeletal system.
Additionally, HSS may involve dental abnormalities, such as missing teeth or abnormal tooth development. These can be coded using codes from the K00-K14 range, which pertain to diseases and disorders of the oral cavity.
It is important to note that ICD-9 codes are no longer in use since the transition to ICD-10 in October 2015. However, for reference, the closest ICD-9 codes that may have been used for HSS-related features include 756.0 for anomalies of the face and 759.89 for other specified congenital anomalies.
In conclusion, Hallermann-Streiff syndrome does not have a specific ICD-10 code, but individual features and associated abnormalities can be coded using appropriate ICD-10 codes related to facial anomalies, musculoskeletal deformities, and dental abnormalities.
The most notable facial features of HSS include a small jaw, beaked nose, sunken eyes, and a thin bird-like appearance. These can be coded using specific facial anomaly codes such as Q18.1 for micrognathia (small jaw), Q30.0 for congenital malformation of the nose, and Q10.2 for microphthalmos (abnormally small eyes).
HSS is also associated with various systemic abnormalities. For instance, individuals with HSS often have skeletal abnormalities like a shortened stature or limb deformities. These can be coded using codes from the Q65-Q79 range, which cover congenital deformities of the musculoskeletal system.
Additionally, HSS may involve dental abnormalities, such as missing teeth or abnormal tooth development. These can be coded using codes from the K00-K14 range, which pertain to diseases and disorders of the oral cavity.
It is important to note that ICD-9 codes are no longer in use since the transition to ICD-10 in October 2015. However, for reference, the closest ICD-9 codes that may have been used for HSS-related features include 756.0 for anomalies of the face and 759.89 for other specified congenital anomalies.
In conclusion, Hallermann-Streiff syndrome does not have a specific ICD-10 code, but individual features and associated abnormalities can be coded using appropriate ICD-10 codes related to facial anomalies, musculoskeletal deformities, and dental abnormalities.
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
