Our Mission
To accelerate the diagnosis of rare diseases by empowering clinicians with advanced AI and intuitive workflows.
Precision Extraction
Sanjeevni uses state-of-the-art NLP models to identify Human Phenotype Ontology (HPO) terms from clinical notes with high accuracy.
Patient-Centered
We bridge the gap between patients and doctors, allowing patients to securely submit evidence directly to their clinician's dashboard.
Bayesian Scoring
Our diagnostic engine leverages the Orphanet database to calculate differential diagnosis probabilities based on matched phenotypes.
The Diagnostic Odyssey
For millions of patients with rare diseases, the journey to a correct diagnosis takes an average of five to seven years. This "diagnostic odyssey" is marked by misdiagnoses, unnecessary tests, and prolonged suffering. The sheer volume of known rare diseases—over 7,000—makes it impossible for any single clinician to recognize every phenotype.
Sanjeevni was built to change this. By structuring unstructured clinical data into standardized HPO terms and comparing those against vast medical ontologies in real-time, we provide doctors with the computational support they need to consider the rarest of possibilities.