DISEASES

Disease-gene associations mined from literature

Human genes for steatocystoma multiplex

Steatocystoma multiplex [DOID:0111556]

A sebaceous gland disease characterized by the presence of multiple benign sebaceous cysts that has_material_basis_in heterozygous mutation in KRT17 on chromosome 17q21.2.

Synonyms:  steatocystoma multiplex,  DOID:0111556,  steatocystoma multiplexes,  multiple sebaceous cysts,  sebocystomatosis ...