About: McLeod syndrome

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An Entity of Type : owl:Class, within Data Space : demo.openlinksw.com associated with source document(s)

Attributes	Values
type	Class
subClassOf	X-linked monogenic disease neuroacanthocytosis nodeID://b50946094
label	McLeod syndrome
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0112107
database_cross_reference	GARD:10731 MESH:C564038 OMIM:300842 ORDO:59306 SNOMEDCT_US_2021_09_01:234411007 UMLS_CUI:C0398568
has_exact_synonym	MLS McLeod neuroacanthocytosis syndrome McLeod type neuroacanthocytosis X-linked McLeod syndrome McLeod syndrome with or without chronic granulomatous disease
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	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.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50946095

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