GeneReviews, an international point-of-care resource for busy clinicians, provides clinically relevant and medically actionable information for inherited conditions in a standardized journal-style format, covering diagnosis, management, and genetic counseling for patients and their families. Each chapter in GeneReviews is written by one or more experts on the specific condition or disease and goes through a rigorous editing and
GeneReviews currently comprises 851 chapters and has more than five million users annually.
The two general formats for GeneReviews are: chapters focused on a single gene or phenotype (~95%) and overviews summarizing causes of common genetic conditions (e.g., deafness and hearing loss, Alzheimer disease) (~5%).
To ensure continuing relevant and medically actionable content, each GeneReviews chapter is
Genetic counseling and testing terms used in GeneReviews are hyperlinked to definitions in the GeneReviews
GeneReviews are indexed in PubMed.
Note: For a variety of reasons, GeneReviews occasionally removes chapters from the active website. Click
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