Short answer · Medically reviewed summary · Last updated: 2023-07-10
Multiple Sulfatase Deficiency (MSD) is a rare genetic disorder characterized by the deficiency of multiple sulfatase enzymes. Unfortunately, as of now, there is no specific ICD10 code exclusively dedicated to MSD.
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ICD10 code of Multiple Sulfatase Deficiency and ICD9 code
ICD-10 and ICD-9 codes for Multiple Sulfatase Deficiency, with classification details for clinicians, coders and patients.
Multiple Sulfatase Deficiency (MSD) is a rare genetic disorder characterized by the deficiency of multiple sulfatase enzymes. Unfortunately, as of now, there is no specific ICD10 code exclusively dedicated to MSD. However, it can be classified using broader codes that encompass lysosomal storage disorders or specific sulfatase enzyme deficiencies. For instance, E75.2 denotes "Other sphingolipidosis" in the ICD10 classification, which can be used to indicate MSD.
In terms of ICD9 coding, it is important to note that ICD9 has been replaced by ICD10 coding system. Therefore, as MSD is not specifically listed in ICD10, there is no direct ICD9 code available. However, in ICD9, related codes such as 272.7 ("Other disorders of lipoid metabolism") or 277.89 ("Other specified disorders of metabolism") might have been used to categorize MSD.
It is crucial to consult with a healthcare professional or a certified medical coder for accurate coding and classification of Multiple Sulfatase Deficiency based on the most up-to-date coding guidelines and resources.
In terms of ICD9 coding, it is important to note that ICD9 has been replaced by ICD10 coding system. Therefore, as MSD is not specifically listed in ICD10, there is no direct ICD9 code available. However, in ICD9, related codes such as 272.7 ("Other disorders of lipoid metabolism") or 277.89 ("Other specified disorders of metabolism") might have been used to categorize MSD.
It is crucial to consult with a healthcare professional or a certified medical coder for accurate coding and classification of Multiple Sulfatase Deficiency based on the most up-to-date coding guidelines and resources.
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
