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ICD-10-CM Codes Browse (Tabular) Diagnostic External Drug Neoplasm

D72.0 – Genetic anomalies of leukocytes

Overview

Coding Notes

Active
Billable, valid for HIPAA-covered transactions

Type 1 Excludes

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

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

GEM Conversion to ICD-9 CM

Fs: 00000 – Genetic anomalies of leukocytes

MDC / MS-DRG Reference

MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH MCC
MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH CC
MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITHOUT CC/MCC

Back Reference of Diagnostic Codes

Alder (-Reilly) anomaly or syndrome (leukocyte granulation) D72.0
Anomaly, anomalous (congenital) (unspecified type) Q89.9
Alder (-Reilly) (leukocyte granulation) D72.0
granulation or granulocyte, genetic (constitutional) (leukocyte) D72.0
Hegglin's D72.0
hypersegmentation of neutrophils, hereditary D72.0
Jordan's D72.0
leukocytes, genetic D72.0
granulation (constitutional) D72.0
May (-Hegglin) D72.0
Pelger-Huët (hereditary hyposegmentation) D72.0
Dohle body panmyelopathic syndrome D72.0
Dysgenesis
reticular D72.0
Hegglin's anomaly or syndrome D72.0
Hypersegmentation, leukocytic, hereditary D72.0
Hyposegmentation, leukocytic, hereditary D72.0
Inclusion
azurophilic leukocytic D72.0
Jordan's anomaly or syndrome D72.0
Leukomelanopathy, hereditary D72.0
May anomaly or syndrome (-Hegglin) D72.0
Neutrophilia, hereditary giant D72.0
Pelger-Huët anomaly or syndrome D72.0
Syndrome See also Disease
Alder's D72.0
Döhle body-panmyelopathic D72.0
Hegglin's D72.0
May (-Hegglin) D72.0
Pelger-Huet D72.0

Sibling Codes

Eosinophilia
Other specified disorders of white blood cells
Disorder of white blood cells, unspecified

Parent Sibling Codes

Neutropenia
Functional disorders of polymorphonuclear neutrophils
Other disorders of white blood cells
Diseases of spleen
Methemoglobinemia
Other and unspecified diseases of blood and blood-forming organs
Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue
Other disorders of blood and blood-forming organs in diseases classified elsewhere
Intraoperative and postprocedural complications of the spleen

View in Tabular

Code Title
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
Type 1 Excludes
Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)

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