Monarch RESTful API
Monarch Phenotype Grid Widget
Phenotype Curation Guidelines
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Specific feedback from users like you is essential to guide future development and improvement of the Monarch experience. We welcome you to answer the questions below and/or contact us via links below.
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The Monarch Initiative
Patient Variant Analysis
Combine genotype and phenotype data across species for patient variant prioritization, functional annotation and pathogenicity determination.
Exome Tool Suite
Securely share & discuss patients with colleagues all around the world.
Use our text mining engines to annotate phenotypes/diseases in your free text. Then optionally compare those phenotypes across species to find candidate models of disease.
Find literature relevant to a set of phenotypes of interest
Phenotype PubMed Browser
Find models and diseases similar to a set of abnormal phenotypes of interest and then visualize their overlap.
Go to Phenotype Analysis
News and Events
Save the Date: Symposium on Linking Disease Model Phenotypes to Human Conditions
Why the Human Phenotype Ontology?
What NLM should think about
How to annotate a patient's phenotypic profile
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