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D72.0 - Genetic anomalies of leukocytes


The ICD 10 Code for Genetic anomalies of leukocytes is listed as D72.0.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.

ICD 10 CM Field Value
Diagnosis Code: D72.0
Description: 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-Hu
Diagnostic Related Groups
(MS-DRG v30.0)
808 - Major Hematol/immun Diag Exc Sickle Cell Crisis & Coagul W Mcc
809 - Major Hematol/immun Diag Exc Sickle Cell Crisis & Coagul W Cc
810 - Major Hematol/immun Diag Exc Sickle Cell Crisis & Coagul W/o Cc/mcc
Chapter Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
Block Other disorders of blood and blood-forming organs (D70-D77)
Parent D72 - Other disorders of white blood cells
ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD 9 Dx Code: 288.2 - Genetic anomalies of leukocytes
ICD-10-CM Siblings (same level / similar specificity) of D72.0:
D72.1 - Eosinophilia
D72.8 - Other specified disorders of white blood cells
D72.9 - Disorder of white blood cells, unspecified