Chédiak-Higashi syndrome

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Name:
Chédiak-Higashi syndrome
Description:
Chédiak-Higashi syndrome (CHS) is a rare severe genetic disorder generally characterized by partial oculocutaneous albinism (OCA, see this term), severe immunodeficiency, mild bleeding, neurological dysfunction and lymphoproliferative disorder. A classic, early-onset form and an attenuated, later-onset form (Atypical CHS; see this term) have been described.
ORPHAcode:
167
Synonyms:
Chédiak-Higashi disease
Chédiak-Higashi-Steinbrink syndrome
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14