Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:00352930n
Noun Concept
Categories: Cytoskeletal defects, Rare diseases, Noninfectious immunodeficiency-related cutaneous conditions, IUIS-PID table 3 immunodeficiencies
EN
Wiskott-Aldrich syndrome  Wiskott–Aldrich syndrome  Aldrich Syndrome  Eczema-Thrombocytopenia-Immunodeficiency Syndrome  Eczema thrombocytopenia immunodeficiency syndrome
EN
Wiskott–Aldrich syndrome is a rare X-linked recessive disease characterized by eczema, thrombocytopenia, immune deficiency, and bloody diarrhea. Wikipedia
Definitions
Relations
Sources
EN
Wiskott–Aldrich syndrome is a rare X-linked recessive disease characterized by eczema, thrombocytopenia, immune deficiency, and bloody diarrhea. Wikipedia
An X-linked recessive disease Wikipedia Disambiguation
Rare disease Wikidata
IS A
rare disease
skin disease
syndrome
combined immunodeficiencies
GENETIC ASSOCIATION
WIPF1
WAS
HEALTH SPECIALTY
immunology
Wikipedia
EN
Wiskott–Aldrich syndrome
Wikidata
EN
Wiskott-Aldrich syndrome
Wikipedia Redirections
EN
Wiscott aldrich, Wiskott-Aldrich, Wiskott-Aldrich syndrome, Wiskott-Aldridge syndrome, Wiskott aldrich, Wiskott aldrich syndrome
Wikidata Alias
EN
Aldrich Syndrome, Eczema-Thrombocytopenia-Immunodeficiency Syndrome, Eczema thrombocytopenia immunodeficiency syndrome, IMD 2, Immunodeficiency 2, WAS, WISKOTT-ALDRICH SYNDROME, WISKOTT-ALDRICH SYNDROME; WAS, Wiskott-Aldrich Syndrome 1, Wiskott Aldrich syndrome, Wiskott 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