Now in clinical beta
Rare diseases, decoded.
Clinical notes, photos, lab reports, and genetic evidence reviewed by the doctor before scoring.
Doctor-reviewed AI
AI suggests phenotypes; clinicians decide what enters scoring.
Capture clinical inputs
Use notes with voice, clinical photos, lab reports, and manual genetic evidence in one case.
How it works
AI suggests HPO findings
Notes, photos, and labs produce phenotype suggestions that stay pending until the doctor accepts them.
How it works
Score accepted evidence
Only accepted HPO findings and reviewed genetic evidence enter the deterministic differential ranking.
How it works
Review and write the referral
See top differentials, missing findings, differentiating clues, and an editable referral letter.
How it worksWorkflow
From input to insight in seconds.
Sanjeevni turns clinical inputs into doctor-reviewed HPO findings, then matches accepted evidence against rare disease knowledge graphs.
Technology
Four clinical inputs. One reviewed differential.
The doctor stays in the loop: AI suggests, the clinician accepts, Sanjeevni scores.
01
Capture clinical inputs
Use notes with voice, clinical photos, lab reports, and manual genetic evidence in one case.
02
AI suggests HPO findings
Notes, photos, and labs produce phenotype suggestions that stay pending until the doctor accepts them.
03
Score accepted evidence
Only accepted HPO findings and reviewed genetic evidence enter the deterministic differential ranking.
04
Review and write the referral
See top differentials, missing findings, differentiating clues, and an editable referral letter.
05
Generate Referral Letter
Automatically convert complex multi-modal evidence into professional, clinician-ready referral letters in seconds.
Science
Orphanet
7,000+ diseases with curated phenotype-gene associations
HPO Ontology
Human Phenotype Ontology with information content scoring
ClinVar
Manual gene evidence connected to curated disease associations
Deterministic
Transparent, auditable scoring
HIPAA & Security
Enterprise grade data protection
Every phenotype is traceable to notes, images, lab reports, or genetic context before it contributes to scoring.
Evidence audit
Accepted HPO terms drive deterministic ranking instead of opaque black-box diagnosis claims.
Transparent scoring
The final output is structured for real referral work, not just a demo result screen.
Referral workflow
Start diagnosing today.
Use Sanjeevni to convert messy clinical evidence into reviewable rare-disease differentials.
Clinical notes, photos, lab reports, and genetic evidence reviewed by the doctor before scoring.
Now in clinical beta