Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 7 of 7 for Autosomal recessive congenital ichthyosis
  1. Nonbullous congenital ichthyosiform erythroderma 
    ... NBIE NCIE Nonbullous ichthyosiform erythroderma Genetic Testing Registry: Autosomal recessive congenital ichthyosis 10 Genetic Testing Registry: Autosomal recessive congenital ichthyosis ...
    https://medlineplus.gov/...ous-congenital-ichthyosiform-erythroderma - Genetics
  2. Harlequin ichthyosis 
    ... not show signs and symptoms of the condition. Autosomal recessive congenital ichthyosis 4B Harlequin baby syndrome HI Ichthyosis congenita, harlequin ...
    https://medlineplus.gov/genetics/condition/harlequin-ichthyosis - Genetics
  3. Lamellar ichthyosis 
    ... Ichthyoses, lamellar Ichthyosis, lamellar LI Genetic Testing Registry: Autosomal recessive congenital ichthyosis 3 Genetic Testing Registry: Autosomal recessive congenital ichthyosis ...
    https://medlineplus.gov/genetics/condition/lamellar-ichthyosis - Genetics
  4. Epidermolytic hyperkeratosis 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, ... Registry: Epidermolytic ichthyosis Autosomal ...
    https://medlineplus.gov/.../condition/epidermolytic-hyperkeratosis - Genetics
  5. Sjögren-Larsson syndrome 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ... Genetic Testing ...
    https://medlineplus.gov/genetics/condition/sjogren-larsson-syndrome - Genetics
  6. DOLK-congenital disorder of glycosylation 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition. CDG1M Congenital disorder of glycosylation, type Im DK1 deficiency Dolichol ...
    https://medlineplus.gov/...dolk-congenital-disorder-of-glycosylation - Genetics
  7. Trichothiodystrophy 
    ... RNF113A TARS1 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ... disorder. The parents of an individual with an autosomal recessive condition each carry one copy of the altered ...
    https://medlineplus.gov/genetics/condition/trichothiodystrophy - Genetics