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
Alder syndrome
Alders syndrome
Chediak higashi syndrome
Chédiak-higashi syndrome
Genetic anomaly of leukocyte
Hereditary giant neutrophilia
Hereditary hypersegmentation
Hypersegmentation
Hypersegmentation, hereditary
Leukocyte adhesion deficiency – type 1
Leukocyte adhesion deficiency – type 2
Leukocyte adhesion deficiency type 1
Leukocyte adhesion deficiency type 2
Leukocyte disorder, genetic
May hegglin anomaly
Pelger-huet anomaly
Pelger-huët anomaly
Pelger-huît anomaly
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.
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; transmitted by autosomal recessive inheritance and a similar disorder occurs in the beige mouse, the aleutian mink, and albino hereford cattle.
D72.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
The 2023 edition of ICD-10-CM D72.0 became effective on October 1, 2022.
This is the American ICD-10-CM version of D72.0 – other international versions of ICD-10 D72.0 may differ.