Genetic anomalies of leukocytes
Billable / specificHCC V28 115
D72.0 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
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
Not coded here — never report together with this code.
Excludes2
Not included here — may be reported together when both conditions exist.
- autoimmune disease (systemic) NOS (M35.9) (from D72)
- certain conditions originating in the perinatal period (P00-P96) (from D72)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D72)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D72)
- endocrine, nutritional and metabolic diseases (E00-E88) (from D72)
- human immunodeficiency virus [HIV] disease (B20) (from D72)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from D72)
- neoplasms (C00-D49) (from D72)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D72)
- neutropenia (D70) (from D72)
Also known as
- 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
- Alder
- Anomaly, anomalous, Alder
- Anomaly, anomalous, granulation or granulocyte, genetic
- Anomaly, anomalous, Hegglin's
- Anomaly, anomalous, hypersegmentation of neutrophils, hereditary
- Anomaly, anomalous, Jordan's
- Anomaly, anomalous, leukocytes, genetic
- Anomaly, anomalous, leukocytes, genetic, granulation
- Anomaly, anomalous, May
- Anomaly, anomalous, Pelger-Huët
- Dohle body panmyelopathic syndrome
- Dysgenesis, reticular
- Hegglin's anomaly or syndrome
- Hypersegmentation, leukocytic, hereditary
- Hyposegmentation, leukocytic, hereditary
Parent code
- D72Other disorders of white blood cellsHeader