| Monarch Initiative |
Monarch is a system that allows for cross-species disease discovery, and Mondo was initially developed for the Monarch Initiative and is used for integrating disease data across species. |
| Biolookup |
The Biolookup Service provides metadata and ontological information about biomedical entities based on their compact identifiers (CURIEs). |
| ClinGen |
ClinGen is a curated database of clinically relevant genes and variants. Mondo is used annotating diseases associated with gene variants. |
| Critcal Path Institute |
An independent nonprofit, public-private partnership with the U.S. Food and Drug Administration (FDA) focused on the medical product development process. |
| European Bioinformatics Institute (EBI) |
EBI uses Mondo as the primary ontology for disease concepts integrated into the Experimental Factor Ontology (EFO) for integration of data across EBI. Mondo is used for disease annotations in EBI resources, Open Targets, GWAS catalog and Euro-Bioimaging. |
| European Joint Programme on Rare Diseases |
An Europe-based information resource for rare diseases. |
| Euro-Bioimaging |
Provides access to bioimaging technologies, training and data services. Mondo is used for disease annotations. |
| Exscientia |
Exscientia is an AI-driven pharmatech company committed to discovering, designing and developing the best possible drugs in the fastest and most effective manner. |
| Fabric Genomics |
Genome interpretation software for use in rare disease diagnosis. |
| Gabriella Miller Kids First Data Resource Portal |
The Kids First Data Resource Portal is a curated database of clinical and genetic sequence data from pediatric patients with structural abnormalities or childhood cancers, and Mondo is used to structure diagnosis information. |
| Global Alliance for Genomics & Health (GAG4H) |
A policy-framing and technical standards-setting organization that aims to enable responsible genomic data sharing within a human rights framework. |
| Global Genes |
A non-profit organization dedicated to eliminating the burdens and challenges of rare diseases for patients and families globally. |
| HL7 International |
A standards developing organization that provides a comprehensive framework and related standards for the exchange, integration, sharing and retrieval of electronic health information that supports clinical practice and the management, delivery and evaluation of health services. |
| Human Cell Atlas |
A group of researchers who aim to create cellular reference maps with the position, function and characteristics of every cell type in the human body. |
| INDRA |
INDRA (Integrated Network and Dynamical Reasoning Assembler) is an automated model assembly system, originally developed for molecular systems biology and then generalized to other domains. |
| Infertility Disease Database |
A resource for genes, experiments and clinical records related with the infertility diseases. |
| MSeqDR: the Mitochondrial Disease Sequence Data Resource Consortium |
Securely collects and shares data for rare diseases, patients and causative mutations. |
| NCBI ClinVar |
ClinVar aggregates information about genomic variation and its relationship to human health. |
| NCBI MedGen |
MedGen organizes information related to human medical genetics, such as attributes of conditions with a genetic contribution. MedGen maps their disease pages to Mondo IDs. |
| NCI Cancer Research Data Commons |
A cloud-based data science infrastructure that connects data sets with analytics tools to allow users to share, integrate, analyze, and visualize cancer research data to drive scientific discovery. |
| Office of Orphan Products Development (OOPD) at U.S. Food and Drug Administration (FDA) |
The FDA Office of Orphan Products Development (OOPD) supports and advances the development and evaluation of new treatments for rare diseases. |
| OMIA |
Online Mendelian Inheritance in Animals (OMIA) is a catalogue/compendium of inherited disorders, other (single-locus) traits, and genes in 346 animal species. |
| Penn TURBO |
TURBO transforms relational electronic health record (EHR) data into a semantic graph. Mondo is used for disease annotations and integration of disease data. |
| Pharos |
Pharos provides a interface to the Knowledge Management Center (KMC) for the Illuminating the Druggable Genome (IDG) program. Diseases in the Pharos database are maped to Mondo terms and IDs. |
| Pombase |
A comprehensive database for the fission yeast Schizosaccharomyces pombe, providing structural and functional annotation, literature curation and access to large-scale data sets. |
| SunQuest |
Sunquest offers comprehensive laboratory informatics, including laboratory information management systems (LIS/LIMS), and lab analytics solutions for clinical pathology, anatomic pathology, and molecular pathology, including next-generation sequencing (NGS) for precision medicine. |