Bardet-Biedl syndrome 22

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Disease Overview

Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the IFT74 gene.


Synonyms

  • BBS20
  • Bardet-Biedl syndrome 20; BBS20
  • Bardet-Biedl syndrome caused by mutation in IFT74
  • Bardet-Biedl syndrome type 20
  • IFT74 Bardet-Biedl syndrome

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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National Organization for Rare Disorders