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McLeod syndrome (DOID:0112107)
Alliance: disease page
Synonyms: McLeod neuroacanthocytosis syndrome; McLeod syndrome with or without chronic granulomatous disease; McLeod type neuroacanthocytosis; MLS; X-linked McLeod syndrome
Alt IDs: OMIM:300842, MESH:C564038, ORDO:59306, UMLS_CUI:C0398568
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory