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Up to: Hereditary skin disorder · Ichthyosis

Inherited ichthyosis

Mendelian disorders of cornification affecting all or most of integument characterized by hyperkeratosis and/or scaling, caused by an inherited modification of the individual's genome.

6 trials tagged with this condition →

  • Netherton syndrome 15 trials
  • Autosomal recessive congenital ichthyosis 2 trials · 10 incl. sub-types Sub-types →
  • Keratinopathic ichthyosis 0 trials · 7 incl. sub-types Sub-types →
  • Ichthyosis vulgaris 3 trials Sub-types →
  • Recessive X-linked ichthyosis 2 trials Sub-types →
  • Peeling skin syndrome 1 trial Sub-types →
  • IFAP syndrome 0 trials Sub-types →
  • Congenital cataract-ichthyosis syndrome 0 trials
  • Ichthyosis hystrix 0 trials Sub-types →
  • Ichthyosis linearis circumflexa 0 trials
  • Ichthyosis with erythrokeratoderma 0 trials
  • Ichthyosis-oral and digital anomalies syndrome 0 trials
  • Neonatal ichthyosis-sclerosing cholangitis syndrome 0 trials

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