Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:01822130n
Noun Concept
Categories: Rare syndromes, Noninfectious immunodeficiency-related cutaneous conditions, Disturbances of human pigmentation, Autosomal recessive disorders, Syndromes in mammals
EN
Chediak-Higashi syndrome  Chédiak–Higashi syndrome  Albinism immunodeficiency  ChC)diak-Higashi-Steinbrink syndrome  ChC)diak-Higashi disease
EN
Chédiak–Higashi syndrome is a rare autosomal recessive disorder that arises from a mutation of a lysosomal trafficking regulator protein, which leads to a decrease in phagocytosis. Wikipedia
Definitions
Relations
Sources
EN
Chédiak–Higashi syndrome is a rare autosomal recessive disorder that arises from a mutation of a lysosomal trafficking regulator protein, which leads to a decrease in phagocytosis. Wikipedia
Rare autosomal recessive disorder related to lysossomal function and the CHS1 gene Wikidata
IS A
syndrome
autosomal recessive disease
GENETIC ASSOCIATION
Lysosomal trafficking regulator
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
Chédiak–Higashi syndrome
Wikidata
EN
Chediak-Higashi syndrome
Wikipedia Redirections
EN
Albinism immunodeficiency, Chediak-Hegashi Syndrome, Chediak-Higashi disease, Chediak-Higashi syndrome, Chediak Higashi disease, Chediak Higashi syndrome, Chediak–Higashi syndrome, Chédiak-Higashi syndrome, Griscelli disease, Silvery hair syndrome
Wikidata Alias
EN
ChC)diak-Higashi-Steinbrink syndrome, ChC)diak-Higashi disease, CHEDIAK-HIGASHI SYNDROME, CHEDIAK-HIGASHI SYNDROME; CHS, Chediak - Steinbrinck anomaly, Chediak Higashi syndrome, CHS, Chédiak-Higashi-Steinbrink syndrome, Chédiak-Higashi disease, Chédiak-Higashi syndrome, Chédiak–Higashi Syndrome

Please note that, in order to improve your browsing experience on this website, BabelNet® uses various types of cookies, including: browsing functionality, performance and statistical cookies.

By continuing to browse the site you are agreeing to our use of cookies. OK

License