Genetic anomalies of leukocytes D72.0

The ICD10 code for the diagnosis "Genetic anomalies of leukocytes" is "D72.0". D72.0 is a VALID/BILLABLE ICD10 code, i.e it is valid for submission for HIPAA-covered transactions.

  • D72.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2019 edition of ICD-10-CM D72.0 became effective on October 1, 2018.
  • This is the American ICD-10-CM version of D72.0 - other international versions of ICD-10 D72.0 may differ.
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)

Codes: = Billable

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.