D72.0 Genetic anomalies of leukocytes
Instructional Notes:
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D72.0
Description: Genetic anomalies of leukocytes
Exclude1:
- Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
Inclusion Term:
- 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
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D72
Description: Other disorders of white blood cells
Exclude1:
- basophilia (D72.824)
- immunity disorders (D80-D89)
- neutropenia (D70)
- preleukemia (syndrome) (D46.9)
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D70-D77
Description: Other disorders of blood and blood-forming organs (D70-D77)
↓
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D50-D89
Description: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Exclude2:
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)