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Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ichthyosiform Erythroderma, Congenital > Hyperkeratosis, Epidermolytic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ichthyosiform Erythroderma, Congenital > Hyperkeratosis, Epidermolytic
... > Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ichthyosis > Ichthyosiform Erythroderma, Congenital > Hyperkeratosis, Epidermolytic
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ichthyosis > Ichthyosiform Erythroderma, Congenital > Hyperkeratosis, Epidermolytic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Ichthyosis > Ichthyosiform Erythroderma, Congenital > Hyperkeratosis, Epidermolytic
... > Skin and Connective Tissue Diseases > Skin Diseases > Keratosis > Ichthyosis > Ichthyosiform Erythroderma, Congenital > Hyperkeratosis, Epidermolytic

Preferred term

Hyperkeratosis, Epidermolytic  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Bullous Congenital Ichthyosiform Erythroderma
  • Bullous Erythroderma Ichthyosiforme
  • Bullous Erythroderma Ichthyosiformes
  • Bullous Erythroderma Ichthyosiformis Congenita of Brocq
  • Bullous Ichthyosiform Erythroderma
  • Bullous Ichthyosiform Erythroderma Congenital
  • Bullous Ichthyosiform Erythrodermas
  • Congenital Bullous Ichthyosiform Erythroderma
  • Congenital Ichthyosiform Erythroderma, Bullous
  • Epidermolytic Hyperkeratosis
  • Epidermolytic Ichthyosis
  • Erythroderma, Bullous Ichthyosiform
  • Erythroderma Ichthyosiforme, Bullous
  • Erythroderma Ichthyosiformes, Bullous
  • Erythrodermas, Bullous Ichthyosiform
  • Ichthyosiforme, Bullous Erythroderma
  • Ichthyosiform Erythroderma, Bullous
  • Ichthyosiform Erythroderma, Bullous Congenital
  • Ichthyosiform Erythrodermas, Bullous
  • Ichthyosiformes, Bullous Erythroderma

Scope note

  • A form of congenital ichthyosis inherited as an autosomal dominant trait and characterized by ERYTHRODERMA and severe hyperkeratosis. It is manifested at birth by blisters followed by the appearance of thickened, horny, verruciform scales over the entire body, but accentuated in flexural areas. Mutations in the genes that encode KERATIN-1 and KERATIN-10 have been associated with this disorder.

History note

  • 1993(1979); use ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992; for ERYTHRODERMA ICHTHYOSIFORME, BULLOUS use ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992, use SKIN DISEASES, BULLOUS 1979-1990

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URI

http://www.yso.fi/onto/mesh/D017488

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