OBO ID: DOID:0112107
Term Name: McLeod syndrome Search Ontology:
Synonyms:
  • McLeod neuroacanthocytosis syndrome
  • McLeod syndrome with or without chronic granulomatous disease
  • McLeod type neuroacanthocytosis
  • MLS
  • X-linked McLeod syndrome
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. (3)
References:
Ontology: Human Disease   ( DOID:0112107 )
Relationships
is a type of:
OTHER McLeod syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
XK McLeod syndrome 300842
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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