Disease-gene associations mined from literature

Human genes for parotid gland cancer

Parotid gland cancer [DOID:9036]

A peroxisomal disease that is characterized by the reduction or absence of functional peroxisomes in the cells of an individual that has_material_basis_in autosomal recessive inheritance of a mutation in the peroxisome biogenesis factor (PEX) genes.

Synonyms:  parotid gland cancer,  DOID:9036,  cancer of parotid gland,  malignant neoplasm of the Parotid,  malignant tumor of parotid gland (disorder) ...