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Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Albinism > Chediak-Higashi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Albinism > Chediak-Higashi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Albinism > Chediak-Higashi Syndrome
Eye Diseases > Eye Diseases, Hereditary > Albinism > Chediak-Higashi Syndrome
... > Skin and Connective Tissue Diseases > Skin Diseases > Pigmentation Disorders > Hypopigmentation > Albinism > Chediak-Higashi Syndrome
... > Pathological Conditions, Signs and Symptoms > Pathologic Processes > Pigmentation Disorders > Hypopigmentation > Albinism > Chediak-Higashi Syndrome
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Albinism > Chediak-Higashi Syndrome
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Albinism > Chediak-Higashi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Primary Immunodeficiency Diseases > Chediak-Higashi Syndrome
Immune System Diseases > Immunologic Deficiency Syndromes > Primary Immunodeficiency Diseases > Chediak-Higashi Syndrome
Hemic and Lymphatic Diseases > Hematologic Diseases > Leukocyte Disorders > Phagocyte Bactericidal Dysfunction > Chediak-Higashi Syndrome
Immune System Diseases > Immunologic Deficiency Syndromes > Phagocyte Bactericidal Dysfunction > Chediak-Higashi Syndrome

Preferred term

Chediak-Higashi Syndrome  

Type

  • Topical Descriptor

Broader concept

Narrower concepts

Entry terms

  • Chediak Steinbrinck Higashi Syndrome
  • Chediak-Steinbrinck-Higashi Syndrome
  • Chediak-Steinbrinck-Higashi Syndromes
  • Oculocutaneous Albinism with Leukocyte Defect

Scope note

  • 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.

History note

  • 71

In other languages

URI

http://www.yso.fi/onto/mesh/D002609

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