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