The Adam Health Illustrated Encyclopedia includes over 4,000 articles about diseases, tests, symptoms, injuries, and surgeries. It also contains an extensive library of medical photographs and illustrations.
http://www.nlm.nih.gov/medlineplus/encyclopedia.html

Literature-database on Adolescence Health.
http://bases.bireme.br/cgi-bin/wxislind.exe/iah/online/?IsisScript=iah/iah.xis&base=ADOLEC&lang=i

Dtabase about adrenoleukodystrophy, a progressive, genetic disorder, which affects the adrenal glands and the white matter of the nervous system.
http://www.esid.org/

AgeLine abstracts the literature of social gerontology as well as aging-related research from psychology, sociology, social work, economics, public policy, and the health sciences.
http://www.aarp.org/research/ageline/

Collection of documents by the Agency for Healthcare Research and Quality.
http://www.ahrq.gov/clinic/epcix.htm

AIDS Guidelines, provided by AIDSinfo - a service ofthe U.S.Department of HEalth and Human Services.
http://aidsinfo.nih.gov/Guidelines/Default.aspx?MenuItem=Guidelines&Search=On

The Association for Health Information and Libraries in Africa (AHILA) with the technical support of the World Health Organization has produced an international index to African health literature and information sources.
http://indexmedicus.afro.who.int/

ALFRED is designed to store and disseminate frequencies of alleles at human polymorphic sites for multiple populations, primarily for the population genetics and molecular anthropology communities.
http://alfred.med.yale.edu/alfred/index.asp

Database of allergens.
http://allallergy.net/databases/

Database on allergens and epitopes.
http://allergen.csl.gov.uk/

The I.U.I.S. Allergen Nomenclature Sub-committee operates under the auspices of the International Union of Immunological Societies (I.U.I.S.) and the World Health Organisation (W.H.O.). The objectives of the I.U.I.S. Allergen Nomenclature Sub-committee are to ...

Allermatchtm is a website where you can compare the amino acid sequence of a protein with sequences of allergenic proteins.
This website carries out automatically the procedures for predicting the potential allergenicity of proteins by bioinformatics approaches as recommended by the Codex alimentarius and FAO/WHO Expert consultation on allergenicity of foods derived through modern biotechnology.
http://www.allermatch.org/

Alport Syndrome is a progressive renal disease with cochlear and ocular involvement. The most common form (~80%) is inherited in an X-linked pattern. X-linked Alport Syndrome (OMIM #301050) is caused by mutations in the type IV collagen alpha chain 5 (COL4A5). The aim of this database is to record all known variants in the COL4A5 gene and their clinical significance. The GenBank sequence NC_000023.9 is used as the reference sequence. The Human Genome Variation Society nomenclature has been used to describe COL4A5 mutations, as well as original nomenclature described by Zhou et al (1994), which includes 202 nucleotides of 5' UTR. ARUP offers full gene sequencing analysis (test 0051786) for classic X-linked Alport syndrome (80% of mutations) and targeted testing for p.C1564S (c.4692G>A), p.L1649R (c.4946T>G), p.R1677Q (c.5232G>A) mutations for adult type Alport syndrome (test 0051710).
http://www.arup.utah.edu/database/ALPORT/ALPORT_welcome.php

Autoimmune Lymphoproliferative Syndrome Database (ALPSbase): Database of mutations causing human ALPS
http://research.nhgri.nih.gov/alps/

This database is aimed at providing an unbiased, centralized, publicly available and regularly updated collection of genetic association studies performed on AD phenotypes.
http://www.alzforum.org/

The Alzheimer's Disease Clinical Trials Database is a joint project of the U.S. Food and Drug Administration (FDA) and the National Institute on Aging (NIA) maintained by the NIA's Alzheimer's Disease Education and Referral (ADEAR) Center.
http://www.alzheimers.org/trials/index.html

AnAge is a database dedicated to the comparative biology of ageing.
http://genomics.senescence.info/species/index.html

AntiJen is a database system focused on the integration of kinetic, thermodynamic, functional, and cellular data within the context of immunology and vaccinology.
http://www.jenner.ac.uk/antijen/

The ARAMIS Information System for research and development projects in Switzerland is intended to provide information to interested parties about research which is financed or carried out by the Federal Government, to improve co-ordination and to increase transparency in this area. It has been implemented in response to a demand of the Swiss Parliament and the Government.
http://www.aramis-research.ch/e/index.html

Autosomal Recessive Polycystic Kidney Disease (ARPKD) or Polycystic Kidney and Hepatic Disease 1 (PKHD1) is an important cause of childhood renal- and liver-related morbidity and mortality with a proposed incidence of 1:20,000 - 1:40,000 live births.
This Database lists the mutations and polymorphisms of PKHD1.
http://www.humgen.rwth-aachen.de/

Database of chromosomal breakpoints and other genomic features related to autism, provided by the canadian Centre for Applied Genomics and The Hospital for Sick Children in Toronto.
http://projects.tcag.ca/autism/

Database about the brain architecture.
http://brancusi.usc.edu/bkms/

Database about genes relevant to cardiovascular and pulmonary disease.
The BayGenomics gene-trap resource provides researchers with access to thousands of mouse embryonic stem (ES) cell lines harboring characterized insertional mutations in both known and novel genes. Each cell line contains an insertional mutation in a specific gene.
http://baygenomics.ucsf.edu/

Bcipep is a database of experimentally determined linear B-cell epitopes of varying immunogenicity collected from literature and other publicly available databases.
http://bioinformatics.uams.edu/mirror/bcipep/gloss.html

Guidelines on hematology
http://www.bcshguidelines.com

BEKIS is an online database, which provides ready access to information about national and international institutions and activities in the area of bioethics research. Users can find information about: research institutions, research groups, research projects and events.
http://bekis.drze.de/

BELIT is an integrated online database developed by the German Reference Centre for Ethics in the Life Sciences (DRZE) and operated in cooperation with the Information and Documentation Centre for Ethics in Medicine (IDEM, Göttingen), the Interfaculty Centre for Ethics in the Sciences and Humanities (IZEW, Tübingen), the Kennedy Institute of Ethics (KIE, Washington) and the Centre de documentation en éthique des sciences de la vie et de la santé de l'INSERM (CDEI, Paris).
http://www.drze.de/BELIT

The Bioethics Database was created in 1998 and is being updated on a regular basis. It comprises more than 370 bioethics institutions (bioethics committees, commissions, training, research and documentation centres) in over 70 countries, including information on activities and publications. Information is based on replies obtained from a widely distributed questionnaire and has been gathered in cooperation with National Commissions and Permanent Delegations to UNESCO.
http://www.unesco.org/bioethics

The database is constructed under the aegis of the Human Genome Variation Society (HGVS); it is a Locus Specific Database (LSDB).. It deals with mutations in loci of allelic genes that specify the antigens of 28 blood group systems (includes all those for which the molecular basis is defined ) and the allelic variants of those genes. Orthologues of a number of genes are included.
The database is compiled and curated by Olga O. Blumenfeld, Department of Biochemistry and constructed by Santosh Patnaik, Department of Cell Biology, Albert Einstein College of Medicine, New York, NY. Collaborators include Marion E. Reid, Laboratory of Immunochemistry, and Cheng-Han Huang, Laboratory of Biochemistry and Molecular Genetics, New York Blood Center, New York, NY.
http://www.bioc.aecom.yu.edu/bgmut/index.htm

Database about the influences of plants on the human skin.
http://bodd.cf.ac.uk/index.html

The Bookshelf is a growing collection of biomedical books compiled by the NCBI (National Center for Biotechnology Information).
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=Books&itool=toolbar

Mutation registry for X-linked agammaglobulinemia.
http://bioinf.uta.fi/BTKbase/

CAIRSS is a bibliographic database of music research literature in music education, music psychology, music therapy, and music medicine.
http://imr.utsa.edu/CAIRSS.html

Scientific evaluation of complementary and alternative medicine by the National Cancer Institute.
http://www.cancer.gov/cancertopics/treatment/cam

Reliable information on complementary and alternative medicines relating to cancer provided by the European Union (EU).
http://www.cam-cancer.org/

Three databases, the NCI/NCBI SKY/M-FISH & CGH Database, the NCI Mitelman Database of Chromosome Aberrations in Cancer, and the NCI Recurrent Aberrations in Cancer, are now integrated into NCBI's Entrez system as Cancer Chromosomes.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=Home&DB=cancerchromosomes

Database about the human immune response to cancer.
http://www2.licr.org/CancerImmunomeDB/

Each year, the American Cancer Society estimates the number of new cancer cases and deaths expected in the United States in the current year and compiles the most recent data on cancer incidence, mortality, and survival rates based on incidence data from the National Cancer Institute and mortality data from the National Center for Health Statistics.
http://caonline.amcancersoc.org/cgi/content/full/caac.20073v1?ijkey=d919724d94cb93c2fc5e38c96cbbe62cbf088d50

This database contains information on familial hypertrophic cardiomyopathy (FHC)-associated mutations and related data.
http://www.angis.org.au/Databases/Heart/heartbreak.html

CardioSignal was designed for integration of regulatory information on the transcriptional regulation involved in heart development and cardiac hypertrophy.
http://www.cardiosignal.org/

CARDS stands for Computer Access to Research on Dietary Supplements. It is a database of federally funded research projects pertaining to dietary supplements. Currently, CARDS contains projects funded by the United States Department of Agriculture (USDA) and the Institutes and Centers (ICs) of the National Institutes of Health (NIH) beginning with fiscal year 1999, the first year that NIH ICs began reporting research related to dietary supplements.
http://ods.od.nih.gov/Research/CARDS_Database.aspx

CarpeDB is a epilepsy genetics database. It profiles some 400 genes linked to epilepsy in humans, mice, nematodes, and other organisms.
http://www.carpedb.ua.edu/

CASR mutations causing hypercalcemia and/or hyperparathyroidism.
http://www.casrdb.mcgill.ca/

This database is intended to serve as a learning tool to obtain curated information for the design of microarray targets to scan collecting duct tissues (human, rat, mouse).
The database focuses on regulatory and transporter proteins expressed in the collecting duct, but when collecting duct proteins are a member of a larger family of proteins, common additional members of the family are included even if they have not been demonstrated to be expressed in the collecting duct.
http://cddb.nhlbi.nih.gov/cddb/

Cellular Properties Database provides a simple repository for data regarding membrane channels, receptor and neurotransmitters that are expressed in specific types of cells. The database is presently focused on neurons but will eventually include other cell types, such as glia, muscle, and gland cells.
http://senselab.med.yale.edu/senselab/CellPropDB/default.asp

Information about more than 41,000 active industry and government-sponsored clinical trials, as well as new drug therapies in research and those recently approved by the FDA.
http://www.centerwatch.com/

CGED (Cancer Gene Expression Database) is a database of gene expression profile and accompanying clinical information. The data of CGED were obtained through collaborative efforts of Nara Institute of Science and Technology and Osaka University School of Medicine to identify genes of clinical importance. This database offers graphical presentation of expression and clinical data with similarity search and sorting functions. Currently, data of breast, colorectal, and hepatocellular cancers are available. Genes in CGED can be searched by 1) gene names or identifiers, or 2) gene ontology terms or keywords in functional annotations in the SwissProt.
http://lifesciencedb.jp/cged/

The CIRRIE Database currently contains over 24,000 citations of international rehabilitation research published between 1990 and the present.
http://cirrie.buffalo.edu/search/index.php

This exhibit displays hundreds of images from medical and natural history texts, most of which were printed before 1800. They are organized by theme: diagnostics, human body, imaging, instruments, physician-patient culture, portraits, public health, reproduction, reproduction instruments, therapeutics.
http://clendening.kumc.edu/dc/rti/index.html

ClinicalTrials provides regularly updated information about federally and privately supported clinical research in human volunteers. ClinicalTrials gives you information about a trial's purpose, who may participate, locations, and phone numbers for more details.
http://clinicaltrials.gov/

Collection of canadian guidelines.
http://mdm.ca/cpgsnew/cpgs/

The Annotated List of Online Continuing Medical Education, with inks to, and descriptions of, more than 285 Web Sites offering more than 13,000 courses and more than 23,000 hours of CME credit.
http://www.cmelist.com/

CoCoDat contains data about morphology, firing properties, ionic currents, ionic conductances, synaptic currents, and connectivity from published experimental reports along with brain structures, methods, bibliographic references and PubMed IDs.
http://www.cocomac.org/cocodat/

Database about the wiring of the primate brain. The main database contains details of hundreds of tracing studies in their original descriptions.
http://cocomac.org/home.htm

This database aims to record all published accounts of mutations in the genes encoding human collagen types I and III. Mutations of these collagen types result predominantly in osteogenesis imperfecta and Ehlers-Danlos syndrome type IV respectively.
http://www.le.ac.uk/genetics/collagen/

ComBase is a database protocol that encompasses observations of bacterial responses to food environments.
http://wyndmoor.arserrc.gov/combase/Search.aspx

Encyclopaedia of cytokines.
http://www.copewithcytokines.de/cope.cgi

CRIP provides anonymized data on and from human biospecimen available for basic, preclinical and clinical research projects in its database partners’ institutes. Web-based query requires prior user’s registration and is for free for researchers both from academia and industry. CRIP covers data from all disease areas for R&D in molecular and clinical medicine.
http://www.crip.fraunhofer.de/

The Comparative Toxicogenomics Database (CTD) identifies interactions between chemicals and genes/proteins in diverse organisms to elucidate the molecular mechanisms by which environmental chemicals affect human health.
CTD curates chemical-gene/protein interactions from the published literature and integrates diverse data (chemicals, genes/proteins, references, sequences, vertebrate and invertebrate organisms, and Gene Ontology) to facilitate unique cross-species and functional perspectives on toxicogenomic information
http://ctd.mdibl.org/

This british database is maintained by BioMedCentral and it contains two registries:

This database is devoted to the collection of mutations in the CFTR gene and is currently maintained by the laboratory of Lap-Chee Tsui on behalf of the international Cystic Fibrosis genetics research community. It was initiated by the Cystic Fibrosis Genetic Analysis Consortium in 1989 to increase and facilitate communications among CF researchers. The specific aim of the database is to provide CF researchers and other related professionals with up to date information about individual mutations in the CFTR gene.
http://www.genet.sickkids.on.ca/cftr/

DARE is a high quality database with structured abstracts of reviews published in the world wide literature, including otherwise difficultly accessible grey literature.
http://www.crd.york.ac.uk/crdweb/

Developmental and Reproductive Toxicology and Environmental Teratology Information Center - Current and older literature on developmental and reproductive toxicology.
http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?DARTETIC.htm

The database of Genotypes and Phenotypes (dbGaP) was developed to archive and distribute the results of studies that have investigated the interaction of genotype and phenotype. Such studies include genome-wide association studies, medical sequencing, molecular diagnostic assays, as well as association between genotype and non-clinical traits.
http://www.ncbi.nlm.nih.gov/gap

The dbMHC database provides an open, publicly accessible platform for DNA and clinical data related to the human Major Histocompatibility Complex (MHC).
http://www.ncbi.nlm.nih.gov/mhc/MHC.cgi?cmd=init

Deja vu is a database of extremely similar Medline citations. Many, but not all, of which contain instances of duplicate publication and potential plagiarism.
http://spore.swmed.edu/dejavu/

Excellent atlas of dermatology.
http://www.dermis.net/

Diagnosaurus allows you to search 1000+ differential diagnoses by:

Facts about dietary supplements, provided by the NIH, National Institutes of Health.
http://dietary-supplements.info.nih.gov/

Registry of austrian dissertations.
http://media.obvsg.at/dissdb

Registry of Dissertations from Germany.
http://www.iwi-iuk.org/dienste/TheO/

Dissertations from the Karolinska Institute.
http://diss.kib.ki.se/index_en.cfm

The Database of Quantitative Cellular Signaling is a repository of models of signaling pathways.
http://doqcs.ncbs.res.in/

The Dynaweb Internet Server, made by the Duke University, presents historical manuscripts and posters under the topic Medicine and Madison Avenue.
http://scriptorium.lib.duke.edu/dynaweb

EAFUS is a database maintained by the U.S. Food and Drug Administration (FDA) Center for Food Safety and Applied Nutrition (CFSAN) under an ongoing program known as the Priority-based Assessment of Food Additives (PAFA).
http://www.cfsan.fda.gov/~dms/eafus.html

Auditory models and data, provided by Boston's University.
http://earlab.bu.edu/Default.aspx

The NIH Human Embryonic Stem Cell Registry lists the derivations of stem cells that are eligible for federal funding. The purpose of the Registry is to provide investigators with:

EMIC is prepared by the Environmental Mutagen Information Center, Oak Ridge National Laboratory, Oak Ridge, Tennessee (EMIC/ORNL) for the federal government. EMIC covers environmental mutation literature from 1950. The records contain CAS Registry Numbers.
http://toxnet.nlm.nih.gov/help/emichelp2.html#SearchScreen

Literature database for the Eastern Mediterranean Region, including countries such as: Afghanistan, Bahrain, Cyprus, Djibouti, Egypt, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Morocco, Oman, The Occupied Territories, Pakistan, Qatar, Saudi Arabia, Somalia, Sudan, Syria, Tunisia, U.A.E., and Yemen Arab Republic has long been felt by researchers, development agencies, health administrators and planners both inside and outside the Eastern Mediterranean Region. Eastern Mediterranean Regional health and biomedical information sources are not always included in the world's leading bibliographic databases.
http://www.who.int/library/databases/emro/en/

EPIMHC is a relational database of MHC-binding peptides and T cell epitopes that are observed in real proteins. Currently, the database contains 4867 distinct peptide sequences from various sources, including 84 tumor-associated antigens.
http://bio.dfci.harvard.edu/epimhc/

Epitome is a database of all known antigenic residues and the antibodies that interact with them, including a detailed description of residues involved in the interaction and their sequence / structure environments. Additionally, Interactions can be visualized using an interface into Jmol.
http://www.rostlab.org/services/epitome/

ETHMED is a literature database in German and English language in the field of biomedical ethics with an emphasis on ethics in medicine. It contains mainly information from Germany, Austria, and Switzerland.
http://www.dimdi.de/static/de/db/dbinfo/ed93.htm

A literature database made by the Georgetown University.
http://bioethics.georgetown.edu/databases/ethxweb/ethx/index.html

The Alcohol and Alcohol Problems Science Database, commonly referred to as ETOH, is the most comprehensive online resource covering all aspects of alcohol abuse and alcoholism. Produced by the National Institute on Alcohol Abuse and Alcoholism (NIAAA), ETOH contains over 110,000 records and is accessed by both researchers and clinicians worldwide. Included in ETOH are abstracts and bibliographic references to journal articles, books, dissertation abstracts, conference papers and proceedings, reports and studies, and chapters in edited works. Updated monthly, ETOH contains research findings from the late 1960s to the present, as well as historical research literature.
http://etoh.niaaa.nih.gov/expanded.htm

The EyeSite database is an information and modelling resource for families of proteins that function in the eye. Homologues are collected from all species and clustered according to tissue type, function and sequence similarity.
A principal feature of the site is structural annotations,which range from experimentally solved structures to close structural neighbours to distant structure predictions. Many pre-generated homology models are provided.
http://eyesite.cryst.bbk.ac.uk/

Database about the HUS (Haemolytic Uraemic Syndrome); this is a disease associated with microangiopathic haemolytic anemia, thrombocytopenia and acute renal failure. A subgroup of the syndrome is strongly associated with abnormalities within the complement regulator factor H gene.
http://www.fh-hus.org/

FARRP offers ...

The Factor H Associated HUS Mutation Database is a database of mutations within the human complement Factor H protein that are associated with Haemolytic Uraemic Syndrome (HUS).
http://www.FH-HUS.org

The Frequency of Inherited Disorders Database (FIDD) has been established by the University of Wales College of Medicine for use in a clinical context, in medical research, for epidemiological studies and in planning for genetic services.
http://medic.cardiff.ac.uk/fidd/

The fMRI Data Center (fMRIDC) is a respository of neuroimaging data obtained in published studies of cognitive function.
http://www.fmridc.org/f/fmridc

Online library with more then 600 medical textbooks.
http://www.freebooks4doctors.com/

The Function BIRN test bed is working to understand the underlying causes of schizophrenia and to develop new treatments for the disease. The Database is provided by the BIRN, the Biomedical Informatics Research Network.
http://www.birncommunity.org/current-users/function-birn/

Database about Peptides, which are capable of forming amyloid plaques.

The Global Disaster Alert and Coordination System provides near real-time alerts about natural disasters around the world and tools to facilitate response coordination, including media monitoring, map catalogues and Virtual On-Site Operations Coordination Centre
http://www.gdacs.org/

The NIH/FDA Genetic Modification Clinical Research Information System (GeMCRIS) is a comprehensive information resource and analytical tool for scientists, research participants, sponsors, institutional oversight committees, federal officials, and others with an interest in human gene transfer research.
http://www4.od.nih.gov/oba/RAC/GeMCRIS/GeMCRIS.htm

Clinical trials, provided by the NIH Genetic Modification Clinical Research Information System (GeMCRIS).
http://www.gemcris.od.nih.gov/Contents/GC_CT_RPT_MAKER.asp

GenAge ia a database of genes related to human ageing.
http://genomics.senescence.info/genes/index.html

This database is a repository of the genetic variations identified and published in the field of inherited arrhythmogenic diseases and cardiac ion channels.
http://www.fsm.it/cardmoc/

Overview about clinical trials on the field of gene therapy, provided by the Journal of Gene Medicine.
http://www.wiley.co.uk/genmed/clinical/

Genes and Disease is a collection of articles that discuss genes and the diseases that they cause.
http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=gnd

GeneSeeker is a database for the identification of genes underlying human genetic disorders. This requires the combination of data related to cytogenetic localization, phenotypes and expression patterns, to generate a list of candidate genes.
http://www.cmbi.ru.nl/GeneSeeker/

Citations to literature on ethics and public policy issues in genetics.
http://bioethics.georgetown.edu/databases/genethx/gene/index.html

The Genetic Association Database is an archive of human genetic association studies of complex diseases and disorders. The aim of this database is to identify medically relevant polymorphism from the large volume of polymorphism and mutational data.
http://geneticassociationdb.nih.gov/

The Genetics Home Reference is the National Library of Medicine's web site about genetic conditions and the genes responsible for those conditions.
http://ghr.nlm.nih.gov/

The observatory is a system of databases with worldwide coverage in bioethics and other areas of applied ethics in science and technology such as environmental ethics, science ethics, and technology ethics.
http://portal.unesco.org/shs/en/ev.php-URL_ID=6200&URL_DO=DO_TOPIC&URL_SECTION=201.html

Database of gerontological literature.
http://www.dza.de/gerolit/gerolit.html

This site provides data and tools for studying the function of DNA sequences, with an emphasis on those involved in the production of hemoglobin. It includes information about naturally-occurring human hemoglobin mutations and their effects, experimental data related to the regulation of the beta-like globin gene cluster, and software tools for comparing sequences with one another to discover regions that are likely to play significant roles.
http://globin.cse.psu.edu/

GOOGLE's bibliographic tool for scientists and other researchers.
http://scholar.google.com/

The Austrian database for scholarships and research grants is the most comprehensive online database in Austria concerning all research areas. Inner-Austrian grant options for students, graduates and researchers as well as incoming (to Austria) and outgoing (from Austria to ...) grants are offered in this database. Moreover, research allowances, prizes and other funding opportunities can be found. Information is given including details of application conditions (application deadline and place) as well as on duration, allocation and financing of each grant.
http://www.grants.at/

The Database covers the following three main classes of mutant: Point Mutations, Insertions, Deletions
http://hadb.org.uk/WebPages/Database/Quiz/intrquiz.htm

A database of point mutations and short additions and deletions in the factor IX gene.
http://www.kcl.ac.uk/ip/petergreen/haemBdatabase.html

The Human Ageing Genomic Resources (HAGR) are a collection of databases and tools designed to help researchers understand the genetics of human ageing. A major resource in HAGR is the core gene database GenAge, a database of genes related to human ageing. Featuring over 2,000 species, AnAge provides a basis for the comparative biology of ageing.
http://genomics.senescence.info/

The Human Brain Project is multi-agency initiative to construct databases of neuroscience data, and to provide tools for searching and retrieving that data to support research, teaching and education of the public into normal and abnormal functions of the nervous system.
http://ycmi-hbp.med.yale.edu/hbpdb/

Database about human hemoglobin variants and thalassemias.
http://globin.cse.psu.edu/globin/hbvar/

The Heart and Calcium functional Network (HCNet) database is a collection of functional gene modules calculated from the microarray data compendium available from the GEO database. It is a specialized database designed to assist experimentalists for cardiac calcium signaling research by providing the pre-calculated gene clusters and their potential correlation network in heart.
http://sbrg2.gist.ac.kr/hcnet/

Heart and Calcium functional Network (HCNet) is a specialized database for mouse heart and calcium signaling toolkit genes. It contains the functional gene modules pre-calculated from the microarray data compendium using various algorithms for genetic network analyses. First of all, it could relieve the burden of wet-scientists in the related fields from the complex and tedious analyses of the high-throughput genetic data. Eventually, it will serve as a good vehicle for setting up an interesting hypothesis by reviewing the dynamic compilation of functional genetic modules.
http://sbrg2.gist.ac.kr/hcnet/

The HEI Air Quality Database, prepared and maintained by Atmospheric and Environmental Research (AER) Inc, focuses on levels of PM2.5 components and gaseous pollutants at and near sites in the EPA's PM2.5 Chemical Speciation Trends Network (STN) and State, Local and Tribal air monitoring stations (SLAMS).
http://hei.aer.com

The Hematopoiesis Promoter Database (HemoPDB) has been developed as a information resource focused on transcriptional regulation in hematopoiesis. HemoPDB is composed of integral, experimentally defined regulatory information, including TFs, cis-regulatory elements, their target gene promoters and corresponding annotations, with links to supporting published references. Accordingly, the database may be searched by Gene Symbol, GenBank Accession Number, UniGene ID, TF (binding site) Name and lineage or cell type within which a gene is expressed.
http://bioinformatics.wistar.upenn.edu/HemoPDB/

The Human Gene Mutation Database (HGMD) represents an attempt to collate known (published) gene lesions responsible for human inherited disease. This database, whilst originally established for the study of mutational mechanisms in human genes (Cooper and Krawczak 1993), has now acquired a much broader utility in that it embodies an up-to-date and comprehensive reference source to the spectrum of inherited human gene lesions. Thus, HGMD provides information of practical diagnostic importance to (i) researchers and diagnosticians in human molecular genetics, (ii) physicians interested in a particular inherited condition in a given patient or family, and (iii) genetic counsellors.
http://www.hgmd.cf.ac.uk/

List of human genome variation databases. This list was compiled by Rania Horaitis at the Genomic Disorders Research Centre, Melbourne.

The HIV Molecular Immunology Database is an annotated, searchable collection of HIV-1 cytotoxic and helper T-cell epitopes and antibody binding sites. These data are also printed in the HIV Molecular Immunology compendium which is updated yearly and provided free of charge to scientific researchers. The goal of this database is to provide a comprehensive listing of defined HIV epitopes.
The database is operated by the University of California for the US Department of Energy.
http://www.hiv.lanl.gov/content/immunology/index

HIV-Guide provided by the John Hopkins University.
http://hopkins-hivguide.org/

The HIV/SIV Vaccine Trials Database was developed as a tool for compilation, search and comparison of published studies on SIV, HIV and SHIV vaccine trials in nonhuman primates.
http://www.hiv.lanl.gov/cgi-bin/vaccine/public/index.cgi

Database about the HLA-system.
http://bio.dfci.harvard.edu/Database/db_show_hla.html

HMRbase is a manually curated database of Hormones and their Receptors. It is a compilation of sequence data after extensive manual literature search and from publicly available databases. HMRbase can be searched on the basis of a variety of data types such as hormone and receptor description and their names, molecular weight, molecular formula, IUPAC name, smiles, physiochemical properties, post-translational modification, developmental stage, subcellular location, length of the protein sequence, organism name etc. This database has been developed by Dr. GPS Raghava's group at Institute of Microbial Technology, Chandigarh, INDIA.
http://crdd.osdd.net/raghava/hmrbase/

The goal of creating the Human Oral Microbiome Database (HOMD) is to provide the scientific community with comprehensive information o­n the approximately 600 prokaryote species that are present in the human oral cavity. The majority of these species are uncultivated and unnamed, recognized primarily by their 16S rRNA sequences. The HOMD presents a provisional naming scheme for the currently unnamed species so that strain, clone, and probe data from any laboratory can be directly linked to a stably named reference entity. The HOMD links sequence data with phenotypic, phylogenetic, clinical, and bibliographic information. Full and partial oral bacterial genome sequences determined as part of this project and the Human Microbiome Project, are being added to the HOMD as they become available. HOMD offers easy to used tools for viewing all publically available oral bacterial genomes
http://www.homd.org/

HSDB (Hazardous Substances Data Bank) is a scientifically reviewed, factual database containing records for about 4500 toxic chemicals. It contains extensive information in areas as toxicity, environmental fate, human exposure, chemical safety, waste disposal, emergency handling, and regulatory requirements.
http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?HSDB

The HTA database contains information on healthcare technology assessments and is produced in collaboration with the INAHTA Secretariat, based at SBU, Sweden.
The database contains records of ongoing projects being conducted by members of INAHTA as well as publications reporting completed technology assessments carried out by INAHTA members and other health technology assessment organisations. The abstracts in the database are descriptive rather than analytical and do not form critical appraisals of the reports (i.e. the reports have not been evaluated by reviewers from the Centre for Reviews and Dissemination).
http://www.crd.york.ac.uk/crdweb/

Epidemiologic database, which provides life tables.
The Human Life - Table Database has been jointly developed by the Max Planck Institute for Demographic Research, Rostock, Germany, the Department of Demography at the University of California, Berkeley, USA and by the Institut national d'études démographiques, Paris, France.
http://www.lifetable.de

The International Bibliographic Information on Dietary Supplements (IBIDS) database provides access to bibliographic citations and abstracts from published, international, scientific literature on dietary supplements.
The Office of Dietary Supplements (ODS) at the National Institutes of Health produces this database to help consumers, health care providers, educators, and researchers find credible, scientific information on a variety of dietary supplements including vitamins, minerals and botanicals. IBIDS was developed and is maintained through an interagency partnership with the Food and Nutrition Information Center,
http://ods.od.nih.gov/showpage.aspx?pageid=48

The Internet Brain Volume Database is a database of neuroanatomic volume measurements spanning various species, diagnoses, and structures for both individual and group results.
http://www.cma.mgh.harvard.edu/ibvd/

You can download the whole text under ...
http://www.cdc.gov/nchs/data/icd9/draft_i10tabular.pdf (Size: 10 MB)
http://www.cdc.gov/nchs/about/otheract/icd9/icd10cm.htm

An ICSC summarizes essential health and safety information on chemicals for their use at the "shop floor" level by workers and employers in factories, agriculture, construction and other work places.
http://www.ilo.org/public/english/protection/safework/cis/products/icsc/dtasht/index.htm

Database, maintained by the WHO, about clinical trials.
http://apps.who.int/trialsearch/

Toxic concentrations of chemicals.
http://www.cdc.gov/niosh/idlh/intridl4.html

This service is provided by the IFPMA, on behalf of its Member Companies and Associations. The portal has been designed as a single entry allowing you to search for comprehensive information on on-going clinical trials (registry) or results of completed trials (database) conducted by the innovative pharmaceutical industry.
http://clinicaltrials.ifpma.org/

X-linked severe combined immunodeficiency (XSCID or X-SCID) is an immune disorder caused by mutations in the X-linked gene IL2RG, which encodes the common gamma chain (c) of the lymphocyte receptors for interleukin-2 (IL-2) and many other cytokines. A database of human XSCID mutations (IL2RGbase) has been assembled. Information on new mutations may be submitted online.
http://research.nhgri.nih.gov/scid/

The international ImMunoGeneTics information system (IMGT; http://imgt.cines.fr), is a high quality integrated information system specialized in immunoglobulins (IG), T cell receptors (TR), major histocompatibility complex (MHC), and related proteins of the immune system (RPI) of human and other vertebrates, created in 1989, by the Laboratoire d'ImmunoGenetique Moleculaire (LIGM; Universite Montpellier II and CNRS) at Montpellier, France
http://www.ebi.ac.uk/imgt/

IMGT/3Dstructure-DB and IMGT/Structural-Query are a 3D structure database and a tool for immunological proteins. They are part of IMGT, the international ImMunoGenetics information system, a high-quality integrated knowledge resource specializing in immunoglobulins (IG), T cell receptors (TR), major histocompatibility complex (MHC) and related proteins of the immune system (RPI) of human and other vertebrate species, which consists of databases, Web resources and interactive on-line tools.
http://imgt3d.igh.cnrs.fr

Informations about vertebrate immunoglobulin and T cell receptor genes.
http://imgt.cines.fr/cgi-bin/GENElect.jv

The IMGT/HLA Sequence Database is a database for sequences of the human major histocompatibility complex (HLA) and includes the official sequences for the WHO HLA Nomenclature Committee for factors of the HLA System. The IMGT/HLA Sequence Database is part of the international ImMunoGeneTics project (IMGT).
http://www.ebi.ac.uk/imgt/hla/

The Index of Medieval Medical Images (IMMI) was a project funded by the National Library of Medicine and by The Ahmanson Foundation. The mission of the IMMI project was to describe and index the contents of all medieval manuscript images with medical components presently held in North American collections.
The Graphic IMMI is a cooperative project between the Medical History Division of the David Geffen School of Medicine, UCLA and the History & Special Collections Division of the Louise M. Darling Biomedical Library, UCLA.
http://digital.library.ucla.edu/immi/

Informations about the Familial Mediterranean Fever and hereditary autoinflammatory diseases.
http://fmf.igh.cnrs.fr/infevers/

Database on allergens in foods.
http://foodallergens.ifr.ac.uk/

Database about the Proteom of the inner ear.
http://oto.wustl.edu/thc/innerear2d.htm

This site documents the initial period of the discovery and development of insulin, 1920-1925, by presenting over seven thousand page images reproducing original documents ranging from laboratory notebooks and charts, correspondence, writings, and published papers to photographs, awards, clippings, scrapbooks, printed ephemera and artifacts. Drawing mainly on the Banting, Best and related collections housed at the Thomas Fisher Rare Book Library and the Archives and Records Management Services at the University of Toronto, it also includes significant holdings from the Aventis Pasteur (formerly Connaught) Archives, and the personal collection of Dr. Henry Best.
http://digital.library.utoronto.ca/insulin/

The Immuno Polymorphism Database (IPD), was developed in 2003 to provide a system for the study of polymorphism in genes of the immune system. The IPD project was established by the HLA Informatics Group of the Anthony Nolan Research Institute in close collaboration with the European Bioinformatics Institute. IPD consists of the following databases:

The ISRCTN is a simple numeric system for the identification of randomised controlled clinical trials worldwide. The ISRCTN Register will also accept registration of other forms of studies designed to assess the efficacy of healthcare interventions. The ISRCTN scheme simplifies the identification of trials and provides a unique number that can be used to track all publications and reports resulting from each trial.
http://www.controlled-trials.com/isrctn/

A product of the Cincinnati based Toxicology Excellence for Risk Assessment, ITER presents chemical risk information from authoritative groups worldwide, including the U.S. Environmental Protection Agency, the U.S. Agency for Toxic Substances and Disease Registry, Health Canada, the Dutch National Institute of Public Health and the Environment, the International Agency for Research on Cancer, as well as independent parties whose risk values have undergone peer review.
http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?iter.htm

JenPep is a family of relational databases, created by the Edward Jenner Institute for Vaccine Research and supporting the growing community of immunoinformaticians. It contains quantitative data on peptide binding to Major Histocompatibility Complexes (MHCs) and to Transmembrane Peptide Transporter (TAP), as well as an annotated list of T-cell epitopes.
http://www.jenner.ac.uk/Jenpep2/

JSNP is a repository of Japanese Single Nucleotide Polymorphism (SNP) data, begun in 2000 and developed through the Prime Minister’s Millennium Project. The aim of this undertaking is to identify and collate up to 150.000 SNPs from the Japanese population, located in genes or in adjacent regions that might influence the coding sequence of the genes. The project has been carried out by a collaboration between the Human Genome Center (HGC) in the Institute of Medical Science (IMS) at the University of Tokyo and the Japan Science and Technology Corporation (JST).
http://snp.ims.u-tokyo.ac.jp/

The Drugs and Lactation Database (LactMed) is a database of drugs to which breastfeeding mothers may be exposed. Among the data included are maternal and infant levels of drugs, possible effects on breastfed infants and on lactation, and alternate drugs to consider.
http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?LACT

Database about mutations and polymorphisms associated with Lafora progressive myoclonus epilepsy.
http://projects.tcag.ca/lafora/

Database about genes involved in the pathogenesis of Progressive Myoclonus Epilepsy (PME) of the Lafora type.
http://projects.tcag.ca/lafora/

Database of latin-american and caribbean literature on health sciences.
http://bases.bireme.br/cgi-bin/wxislind.exe/iah/online/?IsisScript=iah/iah.xis&base=LILACS&lang=i

The LMD is a MIAME compliant microarray data warehouse based on Stanford Microarray Database and Longhorn Array Database.
http://lungmicroarray.org/lmd.shtml

Collection of databases and e-resources at the Library of Congress.
http://www.loc.gov/rr/ElectronicResources/

Lowe oculocerebrorenal syndrome is an X-linked disorder caused by mutations in the OCRL1 gene, which encodes a 105-kDa Golgi protein with phosphatidylinositol (4,5) bisphosphate 5-phosphatase activity. A database of mutations causing Lowe syndrome has been established. Information on new mutations may be submitted online.
http://research.nhgri.nih.gov/lowe/

NASA's Life Sciences Data Archive (LSDA) contains information and data from space flight experiments funded by the National Aeronautics and Space Administration (NASA).
The experiments were conducted from 1961 to the present time, and include human, animal and plant studies.
http://lsda.jsc.nasa.gov/

This database, made by the University of Wisconsin, Michigan State University and The National Museum of Health and Medicine contains images and information from one of the world's largest collection of well-preserved, sectioned and stained brains of mammals. Viewers can see and download photographs of brains of over 100 different species of mammals (including humans) representing 17 mammalian orders.
http://brainmuseum.org/

MAUDE data represents reports of adverse events involving medical devices. The data consists of all voluntary reports since June, 1993, user facility reports since 1991, distributor reports since 1993, and manufacturer reports since August, 1996.
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/search.cfm

This database has been developed to facilitate the identification and differentiation of syndromic entities. Special attention is given to the type of information which, because of space the limitations of the printed form, is usually limited or completely omitted in the existing reference sources.
http://www.nlm.nih.gov/archive/20061212/mesh/jablonski/syndrome_toc/toc_a.html

Medical literature-database from the Caribbean.
http://bases.bireme.br/cgi-bin/wxislind.exe/iah/online/?IsisScript=iah/iah.xis&base=MedCarib&lang=i

MedHist offers free access to a searchable catalogue of Internet sites and resources covering the history of medicine.
http://medhist.ac.uk/

Merriam-Webster's Medical Dictionary - 60,000 terms, definitions and spelling
http://www.nlm.nih.gov/medlineplus/mplusdictionary.html

PubMed, a service of the National Library of Medicine, includes over 14 million citations for biomedical articles back to the 1950's.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi

The Departments of Defense, Health and Human Services, and Veterans Affairs have worked together to create this library of government-sponsored Gulf War-related research.
http://www.gulflink.osd.mil/medsearch/

Basics about geriatrics.
http://www.merck.com/mrkshared/mm_geriatrics/home.jsp

MeSH is the National Library of Medicine's controlled vocabulary thesaurus. It consists of sets of terms naming descriptors in a hierarchical structure that permits searching at various levels of specificity.
http://www.nlm.nih.gov/mesh/meshhome.html

The MHC Haplotype Project is a framework and resource for association studies of all MHC-linked diseases. It will provide the complete genomic sequences of at least 8 different HLA-homozygous typing haplotypes, their resulting variations (SNPs and indels) and ancestral relationships.
http://www.sanger.ac.uk/HGP/Chr6/MHC/

The Microbial Rosetta Stone Database provides access to up-to-date taxonomic classifications of organisms that cause human diseases, improves the consistency of nomenclature in disease reporting, and provides useful links between different public genomic and public health databases.
http://www.microbialrosettastone.com/

The information in the Mitelman Database of Chromosome Aberrations in Cancer relates chromosomal aberrations to tumor characteristics, based either on individual cases or associations. All the data have been manually culled from the literature by Felix Mitelman, Bertil Johansson, and Fredrik Mertens.
http://cgap.nci.nih.gov/Chromosomes/Mitelman

Medicinal materials from natural sources have been used for centuries in China and other countries. They have been recognized as particularly suitable for treating modern diseases such as cardiovascular diseases, asthma and other long-term illnesses. Substitutes and adulterants are often introduced intentionally or accidentally, thus seriously interfering with their therapeutic effects, even leading to life-threatening poisoning. Medicinal materials are traditionally identified by their organoleptic characteristics and other physical properties. However, the differences among related species are sometimes too minute. Chemical analyses may be affected by the physiological and the storage conditions. With the advancement of molecular biology, DNA barcoding has now become a popular means for identification and authentication of plant and animal species. We have established this DNA barcode database for users to retrieve and analyze DNA sequences of medicinal materials. This website includes DNA sequences and information and key references of the medicinal materials recorded in the Pharmacopoeia of the People’s Republic of China, American Herbal Pharmacopoeia and other related references. Relevant information of common adulterants and substitutes are also listed. This database provides a web-based platform for storage, retrieval, comparison and analysis of DNA sequences, for distinguishing medicinal materials from their common substitutes and adulterants.
http://137.189.51.24/mherbsdb/

ModelDB provides an accessible location for storing and efficiently retrieving compartmental neuron models. ModelDB is tightly coupled with NeuronDB. Models can be coded in any language for any environment, though ModelDB has been initially constructed for use with NEURON and GENESIS. Model code can be viewed before downloading and browsers can be set to auto-launch the models.
http://senselab.med.yale.edu/senselab/ModelDB/default.asp

MHC-Peptide Interaction Database (MPID) provides structural information and characterization of MHC peptide interaction on major histocompatibility complex of both class I and class II.
http://surya.bic.nus.edu.sg/mpidt/

Material Safety Data Sheets (MSDS), regulated under Workplace Hazardous Materials Information System (WHMIS) legislation, for chemical products have been available to workers for many years. However because many laboratory workers, whether in research, public health, teaching, etc., are exposed to not only chemicals but infectious substances as well, there was a large gap in the readily available safety literature for employees. These MSDS are produced for personnel working in the life sciences as quick safety reference material relating to infectious micro-organisms.
http://www.phac-aspc.gc.ca/msds-ftss/index.html

The Mouse Tumor Biology (MTB) Database supports the use of the mouse as a model system of hereditary cancer by providing electronic access to:
Descriptions of tumors (data are organized by strain and organ of tumor origin),
Tumor frequency and latency data,
Information on genetic factors associated with tumors and tumor development,
Tumor pathology reports and images,
References, both published and unpublished, and
Links to related online resources including:
http://tumor.informatics.jax.org/FMPro?-db=TumorInstance&-format=mtdp.html&-view

Informations about complementary remedies.
http://nccam.nih.gov/health/atoz.htm

The database contains published mutations and polymorphisms in the NCL genes together with unpublished data included with permission.
http://www.ucl.ac.uk/ncl/

The database provides structure and structure-function data about brain map transformations in cerebellar systems.
http://www.nesys.uio.no/

Database about microelectrode recordings from cortex and other neurophysiological preparations.
http://neurodatabase.org

Neuromice.org is a consortium of three projects established by NIH to enhance genomic and genetic tools for neuroscience research, by creating new mutant mouse models for neurological/behavioral disorders.
http://www.neuromice.org/

Extensive informations about neurouscular diseases, made by the Neuromuscular Disease Center, Washington University, St. Louis, MO, USA.
http://www.neuro.wustl.edu/neuromuscular/

NeuronDB provides a dynamically searchable database of three types of neuronal properties: voltage gated conductances, neurotransmitter receptors, and neurotransmitter substances. It contains tools that provide for integration of these properties in a given type of neuron and compartment, and for comparison of properties across different types of neurons and compartments.
http://senselab.med.yale.edu/senselab/NeuronDB/default.asp

Collection of Guidelines from Australia. Many of them are outdated, but some of the newer ones are excellent.
http://www.nhmrc.gov.au/

Collection of Guidelines from Great Britain.
http://www.nice.org.uk/

This page provides specialized PubMed searches on healthcare quality and costs.
http://www.nlm.nih.gov/nichsr/hedges/search.html

Excellent structured directory of guidelines. The National Library of Guidelines is a collection of guidelines for the NHS. It is based on the guidelines produced by NICE and other national agencies. The main focus of the Library is on guidelines produced in the UK, but where no UK guideline is available, guidelines from other countries are included in the collection. NICE issues guidelines of very high quality. They are based on a systematic review of the evidence and have extensive consultation not only with clinicians but also with patients and, where relevant, industry.
http://www.library.nhs.uk/guidelinesFinder/Default.aspx

All laureates of the nobel prize in physiology or medicine.
http://nobelprize.org/nobel_prizes/medicine/

This site provides a database about rare diseases.
http://www.rarediseases.org/

Clinical Trials by Novartis.
http://www.novartisclinicaltrials.com/

Nuclide Safety Data Sheets provided by the North Carolina State University.
http://www.ncsu.edu/ehs/radiation/forms/nuclide_sheets.pdf

Collection of nutrition databases, scheduled by the Food Safety Risk Analysis Clearinghouse.
http://www.foodrisk.org/

OdorDB is a database of odor molecules.
http://senselab.med.yale.edu/senselab/OdorDB/default.asp

OdorMapDB is designed to be a database to support the experimental analysis of the molecular and functional organization of the olfactory bulb and its basis for the perception of smell.
http://senselab.med.yale.edu/senselab/OdorMapDB/default.asp

The Ovarian Kaleidoscope database (OKdb) is a collaborative online resource for scientists investigating the ovary. It provides information regarding the biological function, expression pattern, and regulation of genes expressed in the ovary, as well as for the phenotypes associated with their mutation.
http://ovary.stanford.edu/

Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders, with links to literature references, sequence records, maps, and related databases. It is based on the book, Mendelian Inheritance in Man. The online version is updated daily.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=OMIM&cmd=Limits

Excellent ophthalmic case studies.
http://www.meduniwien.ac.at/augen/englisch/steps.htm

Excellent ophthalmic case studies.
http://www.meduniwien.ac.at/augen/englisch/steps.htm

The goal of this atlas is to show multiple examples of important lesions of the oral cavity. One should never diagnose a lesion simply by visually inspecting it. The patient history and physical examination are critically important.
http://www.uiowa.edu/%7Eoprm/AtlasHome.html

The scope of the project includes molecular information pertaining to oral pathogens, bacterial and viral.
http://www.oralgen.lanl.gov/

Olfactory receptors (ORs) are the largest family in the genome, and the first of a widening range of chemosensory receptors (CRs) in other chemosensory organs. ORDB began as a database of vertebrate OR genes and proteins and continues to support sequencing and analysis of these receptors by providing a comprehensive archive with search tools for this expanding family. Because of the associated growth of interest in other CRs, the database has grown over the years to include a broad range of chemosensory genes and proteins, that includes in addition to ORs the taste papilla receptors (TPRs), vomeronasal organ receptors (VNRs), insect olfaction receptors (IORs), Caenorhabditis elegans chemosensory receptors (CeCRs), fungal pheromone receptors (FPRs) [these are informal abbreviations for tracking in ORDB, pending development of consensus nomenclature by the field].
http://senselab.med.yale.edu/senselab/ordb/

Compilation of information on orphan diseases.
http://www.orpha.net

The Occupational Safety and Health Review Commission (OSHRC) is an independent Federal agency created to decide contests of citations or penalties resulting from OSHA inspections of American work places.
http://www.oshrc.gov/index.html

OTseeker is a database that contains abstracts of systematic reviews and randomised controlled trials relevant to occupational therapy.
University of Queensland (School of Health and Rehabilitation Sciences)
University of Western Sydney (School of Exercise and Health Sciences).
http://www.otseeker.com

Panteleimon is a database of medical-biological, chemical-pharmaceutical and chemical publications printed in scientific and scientific-practical journals in Ukraine and Russian Federation since 1998.
http://www.panteleimon.org/

Free, regularly updated surgical pathology outlines with links to journal articles, gross and microscopic images, as well as extensive listings of pathology related jobs, fellowships and conferences.
http://www.pathologyoutlines.com/

PediatricEducation.org is a Pediatric Digital Library and Learning Collaboratory intended to serve as a source of continuing pediatric education
http://www.pediatriceducation.org/

PEDro is the Physiotherapy Evidence Database. It gives access to bibliographic details and abstracts of randomised controlled trials, systematic reviews and evidence-based clinical practice guidelines in physiotherapy.
http://www.pedro.org.au/

Pesticide Fact Sheets - NPIC fact sheets are designed to answer questions that are commonly asked by the general public about pesticides and pesticide related topics. These documents are intended to be educational in nature and helpful to consumers making decisions about pesticide use.
http://npic.orst.edu/npicfact.htm?IRIS

This database contains what are known as sleep quotas for 178 separate references, on 127 different species (as of June 29, 2007), in 46 families, across 17 orders, with additional sleep data on other species being added to the database as they become available. Sleep quotas are essentially time spent in each of the two major sleep states (REM and NREM) per day. There are several lines of evidence that point to the fundamental importance of sleep quotas for an analysis of sleep state function.
http://www.bu.edu/phylogeny/

PubMed Central (PMC) is the U.S. National Library of Medicines digital archive of life sciences journal literature. Access to the full text of articles in PMC is free, except where a journal requires a subscription for access to recent articles.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PMC

Literature database on poisonous plants, provided by the FDA.
http://www.cfsan.fda.gov/~djw/plantox.html

POPLINE® (POPulation information onLINE), the world's largest database on reproductive health, provides more than 300,000 citations with abstracts to scientific articles, reports, books, and unpublished reports in the field of population, family planning, and related health issues.
http://db.jhuccp.org/popinform/expert.html

PsiTri is a database on published and unpublished controlled clinical trials, reporting on treatments and interventions for a wide range of conditions within the field of mental health.
http://psitri.stakes.fi/

Database about mutations and polymorphisms in the PTCH1 gene.
http://www.cybergene.se/PTCH/ptchbase.html

Database made by the NLM, History of Medicine Division.
http://www.nlm.nih.gov/exhibition/visualculture/vchome.html

Database of drugs that prolong the Qt interval
http://www.qtdrugs.org

The RAMEDIS system is a platform independent, web-based information system for rare metabolic diseases based on filed case reports. It was developed in close cooperation with clinical partners to allow them to collect information on rare metabolic diseases with extensive details, e.g. about occurring symptoms, laboratory findings, therapy and molecular data.
http://www.ramedis.de

Database about mutations in the RB1-gene.
http://www.d-lohmann.de/Rb/

The REHABDATA database spans almost 50 years of disability and rehabilitation research. More than 65,000 abstracts are available through this database. The database is provided by the National Rehabilitation Information Center for Independence.
http://www.naric.com/research/rehab/

Rehabilitation information system.
http://www.rehadat.de/

Retroviral insertional mutagenesis in mouse hematopoietic tumors provides a potent cancer gene discovery tool in the post-genome-sequence era. To manage multiple high-throughput insertional mutagenesis screening projects, the Retroviral Tagged Cancer Gene Database was developed.
http://rtcgd.ncifcrf.gov/

This database includes genes and interventions that have been studied with respect to their effects on life-span or age-related neurological diseases.
http://sageke.sciencemag.org/cgi/genesdb

Mutations in sarcomere protein genes are known to cause hypertrophic cardiomyopathy, dilated cardiomyopathy, and other diseases.
http://genetics.med.harvard.edu/~seidman/cg3/index.html

SARS Reference is a medical textbook that provides a comprehensive and up-to-date overview of severe acute respiratory syndrome (SARS).
http://www.sarsreference.com/

Satellog provides the ability to dynamically prioritize repeats based on any of their characteristics (i.e. repeat unit, class, period, length, repeat length percentile rank, genomic co-ordinates), polymorphism profile within UniGene, proximity to or presence within gene regions (i.e. cds, UTR, 15 kb upstream etc.), metadata of the genes they are detected within and gene expression profiles within normal human tissues. Unstable repeats associated with 31 diseases were analyzed in Satellog to evaluate their common repeat properties. The utility of Satellog was highlighted by prioritizing repeats for Huntington's disease and schizophrenia.
http://satellog.bcgsc.ca/

Informations about the human blood group system.
http://jove.prohosting.com/scarfex/blood/groups.html

SDAP is a Web server that integrates a database of allergenic proteins with various bioinformatics tools for performing structural studies related to allergens and characterization of their epitopes.
http://fermi.utmb.edu/SDAP/

Epidemiologic database by the NCI, USA.
http://seer.cancer.gov/

The SIEGE (Smoking Induced Epithelial Gene Expression) database is a clinical resource for compiling and analyzing gene expression data from epithelial cells of the human intra-thoracic airway. This database supports a translational research study whose goal is to profile the changes in airway gene expression that are induced by cigarette smoke
http://pulm.bumc.bu.edu/siegeDB/

Collection of Scottish Guidelines, many of them are outdated.
http://www.sign.ac.uk/

Literature on the scientific, medical, technical, policy, behavioral, legal, and historical aspects of smoking and tobacco use. The database includes abstracts of hard to find conference proceedings and government documents, many with historical significance. Although most items have been published since 1965, several records date back to the 1800s. Made by the Office of Smoking and Health, Centers for Disease Control.
http://apps.nccd.cdc.gov/shrl/QuickSearch.aspx

The Stanley Medical Research Institute online genomics database (SMRIDB) is a web-based system for understanding the genetic effects of human brain disease (i.e. bipolar, schizophrenia, and depression). This database contains fully annotated clinical metadata and gene expression patterns.
https://www.stanleygenomics.org/

While the use of STRs for genetic mapping and identity testing has become widespread among DNA typing laboratories, there is no single place where information may be found regarding STR systems. This web site is an attempt to bring together the abundant literature on the subject in a cohesive fashion to make future work in this field easier. Facts and sequence information on each STR system, population data, commonly used multiplex STR systems, PCR primers and conditions, and a review of various technologies for analysis of STR alleles have been included in this database. Addresses for scientists and organizations working in this area have also been included as well as a comprehensive reference listing of material on STRs used for DNA typing purposes.
http://www.cstl.nist.gov/div831/strbase/

The Stromal Cell Database is a joint project of the laboratories of Kateri Moore and Ihor Lemischka in the Department of Molecular Biology at Princeton University, and Christian J. Stoeckert, Jr. at the Center for Bioinformatics at the University of Pennsylvania.
http://stromalcell.mssm.edu/

The Swiss Life Sciences Database provides access to a very comprehensive directory and information platform comprising data of Life Sciences and Biotechnology companies and institutes in Switzerland including company description, additional information and categorization.
http://www.swisslifesciences.com/swisslifesciences/index.php

This Database contains information on:

Nuclear glossary.
http://glossary.dataenabled.com/

Comprehensive high quality medical encyclopedia.
http://www.merck.com/mrkshared/mmanual/sections.jsp

This database allows visualization of disease and non-disease associated non-synonymous single nucleotide polymorphisms (nsSNPs) and displays geometric and relative entropy calculations as described in Stitziel et. al. (JMB,327(5):1021-1030).
http://gila.bioengr.uic.edu/snp/toposnp/

Extensive array of references to literature on biochemical, pharmacological, physiological, and toxicological effects of drugs and other chemicals.
http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?toxadv

TOXNET is a cluster of databases on toxicology, hazardous chemicals, and related areas. Provided by the NLM, National Library of Medicine:

TRI contains data on the estimated annual releases of toxic chemicals to the environment – air, water, soil, underground injection; amounts transferred off-site for waste treatment; and source reduction and recycling data.
This is a NLM-database.
http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?TRI

This database contains evidence based medical material from more than 60 EBM sites.
http://www.tripdatabase.com/

Extensive assemblage of guidelines, collected by the National Guideline Clearinghouse.
http://www.guidelines.gov

The Atlas of Ultrastructural Neurocytology was created by Josef Spacek, MUDr., DrSc.
http://synapses.clm.utexas.edu/

The Urbana Atlas of Pathology, produced by the University of Illinois College of Medicine at Urbana-Champaign. Legends by Patricia J. O'Morchoe, M.D. Images from material collected by Donald R. Thursh, M.D. and Dr. P. J. O'Morchoe.
Concept, design and implementation by Allan H. Levy, M.D., with the assistance of Ms. Jill Conway. Technical assistance by Ms. Dedra Williams and Ms. Tara Ramanathan.
https://www.med.illinois.edu/m2/pathology/PathAtlasf/titlepage.html

The database contains information on genetically engineered crop plants intended for food or feed that have completed all recommended or required reviews for planting, food, or feed use in the United States.
http://usbiotechreg.nbii.gov/database_pub.asp

VBASE2 is a database of germ-line V genes from the immunoglobulin loci of human and mouse. It presents V gene sequences extracted from the EMBL nucleotide sequence database and Ensembl together with links to the respective source sequences.
http://www.vbase2.org/

Virtual Naval Hospital is a digital library of naval medicine and military medicine and humanitarian medicine.
http://www.vnh.org/

This popular web resource includes over 1900 images along with text, tutorials, laboratory exercises, and examination items for self-assessment that demonstrate gross and microscopic pathologic findings associated with human disease conditions.
http://www-medlib.med.utah.edu/WebPath/webpath.html#MENU

Whonamedit.com is a biographical dictionary of medical eponyms. It presents a complete survey of all medical phenomena named for a person, with a biography of that person. Eventually, this will include more than 15.000 eponyms and more than 6.000 persons.
http://www.whonamedit.com/

WHOLIS is the World Health Organization library database available on the web. WHOLIS indexes all WHO publications from 1948 onwards and articles from WHO-produced journals and technical documents from 1985 to the present. An on-site card catalogue provides access to the pre-1986 technical documents.
http://www.who.int/library/databases/en/

A significant number of Active Pharmaceutical Ingredients (APIs) have been identified in the environment and in surface waters. Data on the environmental hazards associated with these substances are emerging but are still scarce. We have compiled publicly available ecotoxicity data for APIs into a database called WikiPharma.
http://www.miphdatabase.com/

The ability to identify male-specific DNA renders Y-chromosomal STR markers an invaluable addition to the standard panel of autosomal loci used in forensic DNA analysis. Particularly in cases of rape and other sexual assault as well as in kinship testing, Y-STR haplotyping can be extremely informative. However, the utility of Y-STR haplotyping in forensic casework depends strongly on the individuality of the male-specific part of the Y chromosome. Assessing individuality requires optimal Y-chromosomal STR markers which have been approved by the forensic and scientific community.
http://www.ystr.org/