From NIH, Orphanet, OMIM, Human Phenotype Ontology, and IEMbase to ClinicalTrials.gov, PubMed, and many more…
Data shared courtesy of, but not limited to, the following organizations:
ClinicalTrials.gov
ClinicalTrials.gov is a database of privately and publicly funded clinical studies conducted around the world.
EURORDIS
We empower, partner, and advocate for people living with a rare disease in Europe
EveryLife Foundation for Rare Diseases
By activating the patient advocate, we can change public policy and save lives.
Global Genes - Allies in Rare Disease
Committed to providing information, resources and connections to all communities affected by rare disease.
Human Phenotype Ontology
Provides a standardized vocabulary of phenotypic abnormalities encountered in human disease - HPO.
IEMbase
Inborn Errors of Metabolism Knowledgebase
MedlinePlus, National Library of Medicine
MedlinePlus brings together authoritative health information from the National Library of Medicine (NLM), the National Institutes of Health (NIH), and other government agencies and health-related organizations.
National Center for Advancing Translational Sciences
Genetic and Rare Diseases Information Center - NIH.
National Library of Medicine
The world's largest biomedical library and a leader in research in computational health informatics.
National Organization for Rare Disorders
National Organization for Rare Disorders - NORD.
Online Mendelian Inheritance in Man
An Online Catalog of Human Genes and Genetic Disorders - OMIM.
Orphanet
The portal for rare diseases and orphan drugs. "Rare diseases are rare, but rare disease patients are numerous".
PubMed
PubMed® comprises more than 35 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full text content from PubMed Central and publisher web sites.
Rare Diseases Clinical Research Network
Advance medical research on rare diseases.
