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Summary Literature (0)
DOID:2582 - acatalasia

Disease Ontology Definition:A peroxisomal disease characterized by loss of catalase activity in erythrocytes that has_material_basis_in homozygous mutation in the CAT gene on chromosome 11p13.

Synonyms: acatalasemia, deficiency of catalase, deficiency of catalase (disorder),

Xenbase Genes : cat.2, cat.1, cat.3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013571 - acatalasia


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): peroxisomal disease (is_a)