Genomic Medicine

A curated online repository of HGNC-approved gene nomenclature, gene families and more. Unique gene symbols and names to over 37,000 human genes, around 19,000 are protein coding. All approved symbols are stored in the HGNC database. Each symbol is unique and we ensure that each gene is only given one approved gene symbol. It is necessary to provide a unique symbol for each gene so that we and others can talk about them, and this also facilitates electronic data retrieval from publications and databases.

a central location for voluntary submission of genetic test information by providers. The scope includes the test's purpose, methodology, validity, evidence of the test's usefulness, and laboratory contacts and credentials.

The site provides information about federally and privately funded clinical research with human volunteers. A search using a keyword, such as "genetic", can be combined with diseases, conditions, location, treatment, sponsor, and more.

Use simple genetic terms to search this protal across the NLM NCBI databases or use to quickly access NCBI databases such as Nucleotide, Genome, Protein, Gene and many more.

This NCBI reference database integrates information from various species. Search with a gene name or by a genetic disease.

GeneReviews are expert-authored, peer-reviewed disease descriptions focused on clinically relevant and medically actionable information on the diagnosis, management, and genetic counseling of patients and families with specific inherited conditions.

OMIM contains information on all known mendelian disorders and over 15,000 genes. OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries contains links to literature references, sequence records, a clinical synopsis, and related databases such as clinicaltrials.gov, Gene Reviews, and GHR.

GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.

This database is comprised of state statutes and bills introduced during the 2007-2017 U.S. state legislative sessions. The database is reviewed and updated monthly. Searchable topics in the database include employment and insurance discrimination, health insurance coverage, privacy, research, the use of residual newborn screening specimens, and other topics of interest.

NHGRI and the European Bioinformatics Institute (EBI) catalog publications based on genome-wide association studies.

Portal for rare diseases and international orphan drugs.

International research group collaboration building a list of comprehensive functional elements in the human genome.

A free electronic database that attempts to consolidate information on all known clinical and a selected set of pre-clinical molecular biomarkers into a single resource.