Short answer · Medically reviewed summary · Last updated: 2023-07-10
Hereditary spherocytosis is a genetic blood disorder characterized by abnormal red blood cells that are spherical in shape instead of the normal biconcave disc shape. These abnormal cells are more prone to rupture, leading to hemolytic anemia.
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ICD10 code of Hereditary Spherocytosis and ICD9 code
ICD-10 and ICD-9 codes for Hereditary Spherocytosis, with classification details for clinicians, coders and patients.
Hereditary spherocytosis is a genetic blood disorder characterized by abnormal red blood cells that are spherical in shape instead of the normal biconcave disc shape. These abnormal cells are more prone to rupture, leading to hemolytic anemia. The disorder is usually inherited in an autosomal dominant pattern.
In the International Classification of Diseases, 10th Revision (ICD-10), hereditary spherocytosis is assigned the code D58.0. This code falls under the category of "Other hereditary hemolytic anemias," which includes various genetic disorders affecting red blood cells.
On the other hand, in the previous edition of the classification system, the ICD-9 code for hereditary spherocytosis was 282.0. This code was used to classify "Hereditary hemolytic anemias," encompassing different types of inherited anemias caused by abnormalities in red blood cells.
It is important to note that ICD codes are used for medical classification and billing purposes, allowing healthcare providers to communicate and document specific diagnoses. These codes provide a standardized way of identifying and categorizing various diseases, including hereditary spherocytosis.
In conclusion, the ICD-10 code for hereditary spherocytosis is D58.0, while the corresponding ICD-9 code is 282.0. These codes help healthcare professionals accurately identify and manage patients with this genetic blood disorder.
In the International Classification of Diseases, 10th Revision (ICD-10), hereditary spherocytosis is assigned the code D58.0. This code falls under the category of "Other hereditary hemolytic anemias," which includes various genetic disorders affecting red blood cells.
On the other hand, in the previous edition of the classification system, the ICD-9 code for hereditary spherocytosis was 282.0. This code was used to classify "Hereditary hemolytic anemias," encompassing different types of inherited anemias caused by abnormalities in red blood cells.
It is important to note that ICD codes are used for medical classification and billing purposes, allowing healthcare providers to communicate and document specific diagnoses. These codes provide a standardized way of identifying and categorizing various diseases, including hereditary spherocytosis.
In conclusion, the ICD-10 code for hereditary spherocytosis is D58.0, while the corresponding ICD-9 code is 282.0. These codes help healthcare professionals accurately identify and manage patients with this genetic blood 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
