GENA Labs
RESEARCH TOOLS

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.

Try a tool What is GENA 3.0
CLINICAL NOTEANALYZED
PhenoLens by GENA

Fever and joint pain since Monday. No rash.

“fever”Fever
PresentHP:0001945
“joint pain”Arthralgia
PresentHP:0002829
“no rash”Skin rash
AbsentHP:0000988
3 codes · 1 absent · 0 not coded
LOOK UP A DISEASEICD-10-CM FY2026
ICD-10 Map by GENA
Apert syndrome
A specific code existsAngelman syndrome
Use Q93.51Q93.5
Valid and billableApert syndrome
Shared with 153Q87.0
The reverse question573 diseases, one code
Q87.8
8,980 rare diseases mapped · Orphanet · MONDO
LOOK UP A GENEGENCC · 19 GROUPS
Gene Standing by GENA
ACO2
5 groups graded itoptic atrophy 9
They disagreeMONDO:0014571
3 groups, all agreedinfantile cerebellar-retinal degeneration
EstablishedMONDO:0013802
one group onlymitochondrial disease
UnexaminedMONDO:0044970
4 diseases · 1 disputed · GenCC
TOOLS

Live on genalabs.net

Each tool does one job, uses public medical references, and is free to use.

PhenoLens by GENA HPO · PHENOPACKET

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
phenolens.genalabs.net
ICD-10 Map by GENA ORPHANET · MONDO · ICD-10-CM

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.

8,980rare diseases mapped
4,121use a code no claim can carry
icdmap.genalabs.net
Gene Standing by GENA GENCC · CLINGEN

Not every gene–disease link is equally real.

Expert groups grade the evidence behind each one, and they do not always agree. Look up a gene or a disease to see who assessed it, what they concluded — and whether anybody has looked at all.

14.5%of genes carry a disputed link
57%graded by one group or none
genestanding.genalabs.net
HOW IT WORKS

Learn with a tool. Work in GENA 3.0.

01

Open a tool

Each tool answers one question. It runs in your browser, with no account needed.

02

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.

03

Take a case further

Have a real case? Carry your codes into GENA 3.0 for a ranked differential diagnosis and a full workup.

GENA 3.0

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
FOR CLINICIANS
  • 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)