Chediak-Higashi syndrome (Q934034)

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An autosomal recessive disease characterized by oculocutaneous albinism, immune deficiency, coagulation deficiency and neuropathy; it is that has material basis in mutations in the CHS1 gene.
  • Chediak-Higashi syndrome
  • CHS
  • Chediak - Steinbrinck anomaly
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English
Chediak-Higashi syndrome
An autosomal recessive disease characterized by oculocutaneous albinism, immune deficiency, coagulation deficiency and neuropathy; it is that has material basis in mutations in the CHS1 gene.
  • Chediak-Higashi syndrome
  • CHS
  • Chediak - Steinbrinck anomaly

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