Symptom annotation made simple
SAMS is a database and phenotyping tool for precision medicine. Physicians can enter clinical signs
from the Human Phenotype Ontology as well as complete diagnoses, and patients can be
involved by sharing the symptoms
they encounter.
Phenotypic data can be imported, exported and shared as Phenopackets.
SAMS is focused on – but not limited to – rare diseases. It was developed at the Charité and Berlin Institute of Health.