PhenCards: a web server linking human phenotype information to biomedical knowledge

PhenCards is a web server for linking human phenotype information to biomedical knowledge.

Phenotype search
Patient notes

Start typing a phenotype term: fitness, disease or symptom (e.g. cleft palate, epilepsy, Rett syndrome). Our autocompletion will help you.
Your query does not have to match a preexisting term.

Enter your phenotype term query here:

Please enter your phenotype term and submit with "Search," or restart text entry with "Reset."

Here, you can submit patient notes through HTTPS to Doc2HPO for parsing out HPO terms.
By submitting here, you admit these are deidentified notes and take responsibility for the security of PHI.

Patient Description

Sample deidentified clinical notes slightly modified to demonstrate negation feature, but courtesy of Griffin et al. Mol Case Stud. 2016. Submit clinical notes with "Search", or restart text entry with "Reset."

If helpful, cite the paper: Havrilla, J.M., Liu, C., Dong, X., Weng, C., Wang, K. PhenCards: a data resource linking human phenotype information to biomedical knowledge. Genome Med 13, 91 (2021). https://doi.org/10.1186/s13073-021-00909-8

All Rights Reserved @ Wang Genomics Lab 2020 - This information, while from reputable sources, is not to be taken as medical advice, and we accept no liability for doing so. Always discuss with a qualified medical provider.

bookEnter your phenotype term query here:

assignmentPatient Description

Enter your phenotype term query here:

Patient Description