ICD-10-CM Code for Genetic anomalies of leukocytes D72.0

ICD-10 code D72.0 for Genetic anomalies of leukocytes is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .

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Genetic anomalies of leukocytes
Alder (granulation) (granulocyte) anomaly
Alder syndrome
Hereditary leukocytic hypersegmentation
Hereditary leukocytic hyposegmentation
Hereditary leukomelanopathy
May-Hegglin (granulation) (granulocyte) anomaly
May-Hegglin syndrome
Pelger-Huët (granulation) (granulocyte) anomaly
Pelger-Huët syndrome
Excludes1: Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)

D72

Excludes1: basophilia (D72.824)
immunity disorders (D80-D89)
neutropenia (D70)
preleukemia (syndrome) (D46.9)

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Get crucial instructions for accurate ICD-10-CM D72.0 coding with all applicable Excludes 1 and Excludes 2 notes from the section level conveniently shown with each code.
This section shows you chapter-specific coding guidelines to increase your understanding and correct usage of the target ICD-10-CM Volume 1 code.

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