Fever and joint pain since Monday. No rash.
Clinical knowledge, one small tool at a time.
GenaLabs builds free, focused tools that show how diagnosis and medical coding really work. Try one in your browser. When you have a real case, GENA 3.0 takes it further.
Live on genalabs.net
Each tool does one job, uses public medical references, and is free to use.
Turn a clinical note into HPO codes.
Paste or dictate a note. Every phrase is coded, and anything that could not be matched is flagged so nothing is missed.
- Present, absent and history findings
- Export IDs, list or Phenopacket
- Nothing stored
What rare disease coding costs.
Most rare diseases do not have their own ICD-10 code. Look up a disease to see exactly what is lost, and whether a more specific code already exists.
Learn with a tool. Work in GENA 3.0.
Open a tool
Each tool answers one question. It runs in your browser, with no account needed.
Learn from real references
Tools are built on public sources such as the Human Phenotype Ontology, Orphanet, MONDO and ICD-10-CM, and show where every answer comes from.
Take a case further
Have a real case? Carry your codes into GENA 3.0 for a ranked differential diagnosis and a full workup.
Have a case? Take it to GENA 3.0.
GENA 3.0 turns a patient’s symptoms into a ranked differential diagnosis, each backed by a plain-language rationale. Use it as a web app, or connect your EHR through a FHIR-compliant API.
Open GENA 3.0- Ranked differential across 30,408 diseases
- Evidence graph linking findings to diseases
- Disease summaries with citations
- AI consultant for the case
- Suggested next workup
- EHR-ready (SMART on FHIR)