- D72.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM D72.0 became effective on October 1, 2022.
- This is the American ICD-10-CM version of D72.0 – other international versions of ICD-10 D72.0 may differ.
ICD-10-CM D72.0 is grouped within Diagnostic Related Group(s):
- 808 Major hematological and immunological diagnoses except sickle cell crisis and coagulation disorders with mcc
- 809 Major hematological and immunological diagnoses except sickle cell crisis and coagulation disorders with cc
- 810 Major hematological and immunological diagnoses except sickle cell crisis and coagulation disorders without cc/mcc
Applicable To
- 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
Type 1 Excludes
- Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to D72.0:
- Alder (-Reilly) (leukocyte granulation) > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- granulation or granulocyte, genetic (constitutional) (leukocyte) > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- Hegglin\’s > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- hypersegmentation of neutrophils, hereditary > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- Jordan\’s > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- leukocytes, genetic > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- granulation (constitutional) > leukocytes, genetic D72.0
- May (-Hegglin) > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- Pelger-Huët (hereditary hyposegmentation) > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- reticular > Dysgenesis
- azurophilic leukocytic > Inclusion
- Alder\’s > Syndrome
- Döhle body-panmyelopathic > Syndrome
- Hegglin\’s > Syndrome
- May (-Hegglin) > Syndrome
- Pelger-Huet > Syndrome