DISEASES

Disease-gene associations mined from literature

Human genes for acatalasia

Acatalasia [DOID:2582]

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:  acatalasia,  acatalasias,  DOID:2582,  acatalasemia,  deficiency of catalase ...

Linkouts:  OMIM