Wiskott-Aldrich syndrome

Summary

DOID:9169 - Wiskott-Aldrich syndrome

Disease Ontology Definition:A syndrome that is characterized by abnormal immune system function and a reduced ability to form blood clots resulting from a decrease in the number and size of blood cell fragments involved in clotting (microthrombocytopenia).

Synonyms: Wiskott syndrome

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

MIM:

MIM:301000 - wiskott-aldrich syndrome; was
MIM:614493 - wiskott-aldrich syndrome 2; was2

MIM:301000 - wiskott-aldrich syndrome; was

MIM:614493 - wiskott-aldrich syndrome 2; was2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): syndrome (is_a), X-linked monogenic disease (is_a), X-linked recessive disease (is_a)