Short answer · Medically reviewed summary · Last updated: 2023-07-10

WHIM syndrome, also known as warts, hypogammaglobulinemia, infections, and myelokathexis syndrome, is a rare primary immunodeficiency disorder. It is characterized by specific clinical features including warts, recurrent bacterial infections, low levels of certain antibodies (hypogammaglobulinemia), and myelokathexis, which refers to the retention of mature neutrophils in the bone marrow. In terms of coding, the International Classification of Diseases, 10th Revision (ICD-10) provides a specific code for WHIM syndrome.

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ICD10 code of WHIM Syndrome and ICD9 code

ICD-10 and ICD-9 codes for WHIM Syndrome, with classification details for clinicians, coders and patients.

ICD9 and ICD10 codes of WHIM Syndrome
WHIM syndrome, also known as warts, hypogammaglobulinemia, infections, and myelokathexis syndrome, is a rare primary immunodeficiency disorder. It is characterized by specific clinical features including warts, recurrent bacterial infections, low levels of certain antibodies (hypogammaglobulinemia), and myelokathexis, which refers to the retention of mature neutrophils in the bone marrow.

In terms of coding, the International Classification of Diseases, 10th Revision (ICD-10) provides a specific code for WHIM syndrome. The ICD-10 code for WHIM syndrome is D81.810. This code falls under the category of "Other primary immunodeficiencies" (D81) and specifically identifies WHIM syndrome.

On the other hand, the International Classification of Diseases, 9th Revision (ICD-9), which has been replaced by ICD-10, does not have a specific code for WHIM syndrome. Since ICD-9 lacks a unique code for this syndrome, healthcare providers may have used more generalized codes related to immunodeficiency disorders or the specific symptoms of WHIM syndrome when coding for this condition in the past.

It is important to note that accurate coding is crucial for medical records, insurance claims, and statistical analysis. Properly coding WHIM syndrome under ICD-10 (D81.810) helps ensure appropriate identification and tracking of this rare immunodeficiency disorder, aiding in research, treatment, and healthcare planning.
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
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