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acatalasia

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description A congenital disorder resulting from a deficiency in erythrocyte catalase, an enzyme responsible for the breakdown of hydrogen peroxide.
Uniprot Description A metabolic disorder characterized by a total or near total loss of catalase activity in red cells. It is often associated with ulcerating oral lesions. Acatalasemia is inherited as an autosomal recessive trait.
Mondo Term and Equivalent IDs
MONDO:0013571:  acatalasia
EFO:0004144: 
GARD:0000363: 
MESH:D020642: 
NCIT:C84526: 
Orphanet:926: 
SCTID:124202004: 
UMLS:C0268419: