For Centers of
Excellence

Genetico helps clinicians spend less time on data and more time on patients

Document processed
HPO ExtractionAuto
  • HP:0001250 · Seizures
  • HP:0000924 · Skeletal anomaly
  • HP:0004322 · Short stature
Rapid ScoreAI · Ranked
Marfan Syndrome94%
Ehlers-Danlos Synd.67%

The Problem

The Clinical Burden

Clinicians at COEs spend a disproportionate amount of time on documentation, data re-entry, and manual reasoning — time that should go to patient care.

INTAKE

Patient arrives with unstructured notes

Clinician manually reads, interprets, and re-types data from paper records. No standard format exists across referrals.

How It Works

How Genetico Solves It

Clinicians currently use disconnected paper forms, unstructured notes, and ad-hoc reporting. Every consultation starts from scratch. No consistency across the team.

01

CLINICAL STANDARDIZATION

Customizable Clinical Workflow

Structured, guided data capture across the entire consultation — demographics, symptoms, family history, investigations. Consistent across all clinicians in the COE.

40% reduction in consultation documentation time

Patient Intake — Step 3 of 5

HPO TERMS

Seizures HP:0001250×Hypotonia HP:0001290×Ataxia HP:0001251×+ Add term

SYMPTOM ONSET

Infancy (0–2 years)

FAMILY HISTORY

NoneAffected siblingUnknown
Form completion60%
02

DATA CAPTURE

OCR & Report Digitisation

Extract structured clinical and genetic data from scanned lab reports, PDFs, and physical documents. Eliminates manual re-entry and dramatically cuts processing time.

Eliminates time taken for manual transcription

Document Import

lab_report_aiims_2024.pdf

2.4 MB · Uploaded just now

Done
Extracting structured data100%

IDENTIFIED DATA

  • Gene VariantBRCA2 pathogenic c.5946delT
  • PhenotypeHP:0001250 Seizures
  • PhenotypeHP:0000924 Skeletal anomalies
  • Lab ValueCK: 1,240 U/L ↑ elevated
StructuredHPO TaggedRegistry-Ready
03

LONGITUDINAL CARE

Long-term Follow-up Tracking

Structured patient records persist across all visits. Alerts for overdue follow-ups. Longitudinal view of disease progression per patient, automatically updated each visit.

No rebuilding of patient history at each visit

Patient Timeline
AS

Ananya Sharma

ID: GEN-2024-041 · Rare skeletal dysplasia

Active

Jan 2023

Initial Visit

Jun 2023

Follow-up Consult

Dec 2023

Diagnosis Confirmed

Aug 2024

Follow-up Due

PENDING

LAST NOTE — DEC 2023

Skeletal dysplasia confirmed. NPRD report filed. Next review in 8 months.

Follow-up due Aug 2024
Schedule

Results

Measurable Outcomes

Concrete, quantifiable impact across the areas that matter most for Centers of Excellence.

0%BETTER

TIME SAVED

2-3 hrs→Minutes

  • Manual re-entry & HPO searches
  • AI-driven automated extraction
0%BETTER

DIAGNOSIS QUALITY

Memory→RAPID Score

  • Inconsistent, recall-based
  • Evidence-ranked, reproducible
0%BETTER

DATA AVAILABILITY

Siloed→Registry-Ready

  • Zero research output
  • Structured cohort dataset

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