autosomal recessive congenital ichthyosis 1

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Disease Overview

Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the TGM1 gene.


Synonyms

  • ARCI1
  • LI1
  • autosomal recessive congenital ichthyosis 1
  • autosomal recessive congenital ichthyosis type 1
  • bathing suit ichthyosis
  • collodion baby, self-healing
  • collodion fetus
  • collodion foetus
  • desquamation of newborn
  • ichthyosis congenita
  • ichthyosis congenita 2
  • ichthyosis lamellar 1
  • ichthyosis, congenital, autosomal recessive 1
  • ichthyosis, congenital, autosomal recessive 1, with bathing suit distribution
  • ichthyosis, congenital, autosomal recessive type 1
  • ichthyosis, lamellar, 1
  • ichthyosis, lamellar, 1, formerly
  • lamellar exfoliation of newborn
  • lamellar ichthyosis, type 1

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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GeneReviews

GeneReviews has an article on this condition covering diagnosis, management, and inheritance. Each article is written by one or more experts on the specific disease and is reviewed by other specialists. The article contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. The GeneReviews database is managed by the University of Washington.

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