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DOID:0112107 - McLeod syndrome
Disease Ontology Definition:A neuroacanthocytosis characterized by absence of red blood cell Kx antigen, weak expression of Kell red blood cell antigens, acanthocytosis, compensated hemolysis, and involuntary movements that has_material_basis_in mutation in XK on chromosome Xp21.1.
Synonyms: McLeod neuroacanthocytosis syndrome, McLeod syndrome with or without chronic granulomatous disease, McLeod type neuroacanthocytosis, MLS, X-linked McLeod syndrome
Xenbase Genes
:
xk
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee