Diagnosis Code: D72.0

Short Description: Genetic anomalies of leukocytes

Long Description: Genetic anomalies of leukocytes

The code D72.0 is VALID for claim submission

Code Classification:

• Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
  • Other disorders of blood and blood-forming organs (D70-D77)
    • Other disorders of white blood cells (D72)
      • D72.0 Genetic anomalies of leukocytes

Code Version: 2022 ICD-10-CM

Synonyms

• Combined phagocytic defect
• Congenital atrophy of optic nerve
• De Vaal's syndrome
• Defective phagocytic cell adhesion
• Defective phagocytic cell adhesion
• Genetic anomaly of leukocyte
• Genetic anomaly of leukocyte
• Hereditary hypersegmentation
• Hereditary neutrophilia
• Hypersegmentation
• Leukocyte adhesion deficiency
• Leukocyte adhesion deficiency
• Leukocyte adhesion deficiency - type 1
• Leukocyte adhesion deficiency - type 2
• Neutrophilia
• Neutrophilia disorder
• Pelger-Huët anomaly
• Pelger-Huët anomaly
• Pelger-Huët cell
• Pelger-Huët cell
• Reticular dysgenesis
• Reticular dysgenesis
• Reticular dysgenesis with congenital aleukocytosis
• SCID due to absent peripheral T cell maturation
• SCID due to absent peripheral T cell maturation
• SCID due to absent peripheral T cell maturation
• Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome

Diagnostic Related Group(s)

The code D72.0 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Major Hematological And Immunological Diagnoses Except Sickle Cell Crisis And Coagulation Disorders With Mcc (808)
• Major Hematological And Immunological Diagnoses Except Sickle Cell Crisis And Coagulation Disorders With Cc (809)
• Major Hematological And Immunological Diagnoses Except Sickle Cell Crisis And Coagulation Disorders Without Cc/mcc (810)

References to Index of Diseases and Injuries

The code D72.0 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • 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 Notes:
  • Chédiak (-Steinbrinck)-Higashi syndrome (@E70.330*)

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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