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2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of The Blood And Blood-Forming Organs 280-289 > Diseases Of White Blood Cells 288.* > 2008 ICD-9-CM Diagnosis 288.2 Genetic anomalies of leukocytes A form of phagocyte bactericidal dysfunction characterized by unusual oculocutaneous albinism, high incidence of lymphoreticular neoplasms, and recurrent pyogenic infections. In many cell types, abnormal lysosomes are present leading to defective pigment distribution and abnormal neutrophil functions. The disease is transmitted by autosomal recessive inheritance and a similar disorder occurs in the beige mouse, the Aleutian mink, and albino Hereford cattle. A rare autosomal recessive immunodeficiency disorder characterized by abnormal intracellular protein transport. Chediak-Higashi syndrome (CHS) is characterized by immune deficiency; partial oculocutaneous albinism; a bleeding disorder due to deficient platelet dense bodies; neutropenia; neutrophils with impaired chemotaxis and bactericidal activity; recurrent infection; and abnormal natural killer (NK) cell function. CHS may be associated with hepatosplenomegaly, lymphadenopathy, anemia, thrombocytopenia, roentgenologic changes in bones, lungs and heart, and skin and psychomotor abnormalities; it is often fatal in childhood as a result of infection or an accelerated lymphoma-like phase. CHS occurs in mink, cattle, and mice, as well as man. --2004 288.2 is a specific code that can be used to specify a diagnosis 288.2 contains 37 index entries View the ICD-9-CM Volume 1 288.* hierarchy 288.2 also known as: Anomaly (granulation) (granulocyte) or syndrome: Alder's (-Reilly) Chédiak-Steinbrinck (-Higashi) Jordan's May-Hegglin Pelger-Huet Hereditary: hypersegmentation hyposegmentation leukomelanopathy Index entries containing 288.2: Alder's anomaly or syndrome (leukocyte granulation anomaly) 288.2 Alder-Reilly anomaly (leukocyte granulation) 288.2 Anomaly, anomalous (congenital) (unspecified type) 759.9 Alder (-Reilly) (leukocyte granulation) 288.2 Chédiak-Higashi (-Steinbrinck) (congenital gigantism of peroxidase granules) 288.2 granulation or granulocyte, genetic 288.2 constitutional 288.2 leukocyte 288.2 Hegglin's 288.2 hypersegmentation of neutrophils, hereditary 288.2 Jordan's 288.2 leukocytes, genetic 288.2 granulation (constitutional) 288.2 May (-Hegglin) 288.2 pelger-Huët (hereditary hyposegmentation) 288.2 Chédiak-Higashi (-Steinbrinck) anomaly, disease, or syndrome (congenital gigantism of peroxidase granules) 288.2 Disease, diseased - see also Syndrome Chédiak-Steinbrinck (-Higashi) (congenital gigantism of peroxidase granules) 288.2 Döhle body-panmyelopathic syndrome 288.2 Hegglin's anomaly or syndrome 288.2 Hypersegmentation, hereditary 288.2 eosinophils 288.2 neutrophil nuclei 288.2 Hyposegmentation of neutrophils, hereditary 288.2 Inclusion azurophilic leukocytic 288.2 Jordan's anomaly or syndrome 288.2 Leukomelanopathy, hereditary 288.2 May (-Hegglin) anomaly or syndrome 288.2 Neutrophilia, hereditary giant 288.2 Pelger-Huët anomaly or syndrome (hereditary hyposegmentation) 288.2 Phenomenon Pelger-Huët (hereditary hyposegmentation) 288.2 Syndrome - see also Disease Alder's (leukocyte granulation anomaly) 288.2 Béquez César (-Steinbrinck-Chédiak-Higashi) (congenital gigantism of peroxidase granules) 288.2 Chédiak-Higashi (-Steinbrinck) (congenital gigantism of peroxidase granules) 288.2 Döhle body-panmyelopathic 288.2 Hegglin's 288.2 Jordan's 288.2 May (-Hegglin) 288.2 Pelger-Huët (hereditary hyposegmentation) 288.2