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The Human Phenotype Ontology (HPO) provides a standardized vocabulary of phenotypic abnormalities encountered in human disease

LOINC is a common language (set of identifiers, names, and codes) for identifying health measurements, observations, and documents.

A rich and highly specific standardised medical terminology to facilitate sharing of regulatory information internationally for medical products used by humans

The Pharmacogenomics Knowledge Base

SIDER contains information on marketed medicines and their recorded adverse drug reactions.

TargetScan predicts biological targets of miRNAs by searching for the presence of conserved 8mer, 7mer, and 6mer sites that match the seed region of each miRNA

The UMLS integrates and distributes key terminology, classification and coding standards, and associated resources to promote creation of more effective and interoperable biomedical information systems and services, including electronic health records.

UniProt is a freely accessible database of protein sequence and functional information

The 1000 Genomes Project created a catalogue of common human genetic variation, using openly consented samples from people who declared themselves to be healthy.

A comprehensive repository of biomedical ontologies