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Skin and Connective Tissue Diseases > Skin Diseases > Nail Diseases > Pachyonychia Congenita > Steatocystoma Multiplex
... > Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ectodermal Dysplasia > Pachyonychia Congenita > Steatocystoma Multiplex
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ectodermal Dysplasia > Pachyonychia Congenita > Steatocystoma Multiplex
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Ectodermal Dysplasia > Pachyonychia Congenita > Steatocystoma Multiplex
... > Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ectodermal Dysplasia > Pachyonychia Congenita > Steatocystoma Multiplex
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ectodermal Dysplasia > Pachyonychia Congenita > Steatocystoma Multiplex

Preferred term

Steatocystoma Multiplex  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Cyst, Multiple Sebaceous
  • Cysts, Multiple Sebaceous
  • Multiple Sebaceous Cyst
  • Multiple Sebaceous Cysts
  • Multiplex Steatocystoma
  • Multiplex Steatocystomas
  • Sebaceous Cyst, Multiple
  • Sebaceous Cysts, Multiple
  • Steatocystoma, Multiplex
  • Steatocystomas, Multiplex

Scope note

  • A disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations for Pachyonychia congenita, Type 2. Natal teeth involvement is sometimes associated with steatocystoma multiplex.

History note

  • 2013

In other languages

URI

http://www.yso.fi/onto/mesh/D062685

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