D72.0 Genetic anomalies of leukocytes
Billable ICD-10-CM code, FY2026.
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
Excludes1 (never code together)
- Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
Applies from D72 Other disorders of white blood cells
Excludes1 (never code together)
- basophilia (D72.824)
- immunity disorders (D80-D89)
- neutropenia (D70)
- preleukemia (syndrome) (D46.9)
Risk adjustment (HCC)
- CMS-HCC V28: HCC 115 — Specified Immunodeficiencies and White Blood Cell Disorders
- CMS-HCC V22: HCC 47 — Disorders of Immunity
- ESRD V24: HCC 47
MS-DRG index
Defines the logic of DRG(s) 808-810 in MDC 16.
Approximate ICD-9-CM (GEMs)
288.2 Genetic anomalies of leukocytes
Diagnosis Index entries for D72.0
- Alder (-Reilly) anomaly or syndrome (leukocyte granulation)
- Anomaly, anomalous (congenital) (unspecified type) › Alder (-Reilly) (leukocyte granulation)
- Anomaly, anomalous (congenital) (unspecified type) › granulation or granulocyte, genetic (constitutional) (leukocyte)
- Anomaly, anomalous (congenital) (unspecified type) › Hegglin's
- Anomaly, anomalous (congenital) (unspecified type) › hypersegmentation of neutrophils, hereditary
- Anomaly, anomalous (congenital) (unspecified type) › Jordan's
- Anomaly, anomalous (congenital) (unspecified type) › leukocytes, genetic
- Anomaly, anomalous (congenital) (unspecified type) › leukocytes, genetic › granulation (constitutional)
- Anomaly, anomalous (congenital) (unspecified type) › May (-Hegglin)
- Anomaly, anomalous (congenital) (unspecified type) › Pelger-Huët (hereditary hyposegmentation)
- Dohle body panmyelopathic syndrome
- Dysgenesis › reticular
- Hegglin's anomaly or syndrome
- Hypersegmentation, leukocytic, hereditary
- Hyposegmentation, leukocytic, hereditary
- Inclusion › azurophilic leukocytic
- Jordan's anomaly or syndrome
- Leukomelanopathy, hereditary
- May (-Hegglin) anomaly or syndrome
- Neutrophilia, hereditary giant
- Pelger-Huët anomaly or syndrome
- Syndrome › Alder's
- Syndrome › Döhle body-panmyelopathic
- Syndrome › Hegglin's
- Syndrome › May (-Hegglin)
- Syndrome › Pelger-Huet
Nearby codes
D72 Other disorders of white blood cellsD72.0 Genetic anomalies of leukocytes (this code)D72.1 EosinophiliaD72.10 Eosinophilia, unspecifiedD72.11 Hypereosinophilic syndrome [HES]D72.110 Idiopathic hypereosinophilic syndrome [IHES]D72.111 Lymphocytic Variant Hypereosinophilic Syndrome [LHES]