ICD 10 CM Codes

D72.0 Genetic anomalies of leukocytes
Billable Code  is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
GEMS
ICD-10-CM D72.0 converts approximately to:ICD-9-CM
2015 ICD-9-CM 288.2 Genetic anomalies of leukocytes
ICD-10-CM D72.0is grouped within Diagnostic Related Group(s) (MS-DRG v30.0)
808 MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH MCC
809 MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH CC
810 MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITHOUT CC/MCC
Type 1 Excludes
Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
Alternate Description
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
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.D72.0.'
Alder (-Reilly) anomaly or syndrome (leukocyte granulation)
Anomaly, anomalous (congenital) (unspecified type); Alder (-Reilly) (leukocyte granulation)
Anomaly, anomalous (congenital) (unspecified type); granulation or granulocyte, genetic (constitutional) (leukocyte)
Anomaly, anomalous (congenital) (unspecified type); Hegglin's
Anomaly, anomalous (congenital) (unspecified type); hypersegmentation of neutrophils, hereditary
Anomaly, anomalous (congenital) (unspecified type); Jordan's
Anomaly, anomalous (congenital) (unspecified type); leucocytes, genetic
Anomaly, anomalous (congenital) (unspecified type); leucocytes, genetic; granulation (constitutional)
Anomaly, anomalous (congenital) (unspecified type); May (-Hegglin)
Anomaly, anomalous (congenital) (unspecified type); Pelger-Huët (hereditary hyposegmentation)
Dohle body panmyelopathic syndrome
Dysgenesis; reticular
Hegglin's anomaly or syndrome
Hypersegmentation, leukocytic, hereditary
Hyposegmentation, leukocytic, hereditary
Inclusion; azurophilic leukocytic
Jordan's anomaly or syndrome
Leukomelanopathy, hereditary
May (-Hegglin) anomaly or syndrome
Neutrophilia, hereditary giant
Pelger-Huët anomaly or syndrome
Syndrome; Alder's
Syndrome; Döhle body-panmyelopathic
Syndrome; Hegglin's
Syndrome; May (-Hegglin)
Syndrome; Pelger-Huet