Skip to main

Medical Subject Headings (thesaurus)

Search from vocabulary

mapear
anotar
descargar

Concept information

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

Término preferido

Steatocystoma Multiplex  

Notice: Undefined index: in /var/www/html/model/Concept.php on line 545

Tipo

  • mesh:Descriptor

Definición

  • 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.

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Multiple Sebaceous Cysts
  • Multiplex Steatocystoma
  • Sebaceous Cysts, Multiple

En otras lenguas

  • Sébocystomatose

    francés

  • Maladie polykystique épidermique héréditaire
  • Naevus kystiques pilosébacés disséminés
  • Stéatocystomes multiples

URI

http://data.loterre.fr/ark:/67375/JVR-F4MZR5XF-9

Descargue este concepto:

RDF/XML TURTLE JSON-LD Creado 3/7/12, última modificación 18/6/15