Kodex

Code

D72.0

Genetic anomalies of leukocytes

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Hierarchy

D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
- D70-D77 Other disorders of blood and blood-forming organs (D70-D77)
  - D72 Other disorders of white blood cells
    - D72.0 Genetic anomalies of leukocytes
    - D72.1 Eosinophilia
    - D72.8 Other specified disorders of white blood cells
    - D72.9 Disorder of white blood cells, unspecified

Inclusion Terms

D72.0

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

Excludes 1

D72.0

Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
- E70.330 Chediak-Higashi syndrome

D72.824 Basophilia
immunity disorders (D80-D89)
- D80-D89 Certain disorders involving the immune mechanism (D80-D89)
D70 Neutropenia
preleukemia (syndrome) (D46.9)
- D46.9 Myelodysplastic syndrome, unspecified

Excludes 2

autoimmune disease (systemic) NOS (M35.9)
- M35.9 Systemic involvement of connective tissue, unspecified
P00-P96 Certain conditions originating in the perinatal period (P00-P96)
complications of pregnancy, childbirth and the puerperium (O00-O9A)
- O00-O9A Pregnancy, childbirth and the puerperium (O00-O9A)
Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
endocrine, nutritional and metabolic diseases (E00-E88)
B20 Human immunodeficiency virus [HIV] disease
S00-T88 Injury, poisoning and certain other consequences of external causes (S00-T88)
C00-D49 Neoplasms (C00-D49)
symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)