Digital Backbone

Connecting Data, Care, and Collaboration Across the Rare Disease Ecosystem

Who We Are

Trusted by leading institutions including

AIIMS
Delhi
and
adopted
by
CDFD
Hyderabad
for
the
PraGed
Mission
across
the
15
Centres
under
it
, Genetico is building the digital backbone for the rare and genetic disease ecosystem.

Through

IndiGeneUs.AI, our AI-powered clinical genetics platform, we connect patient records, clinical workflows, phenotype data, registries, decision support, analytics, and research into one secure ecosystem.

Genetico enables better clinical decisions, accelerates research, strengthens public health programs, and supports collaboration

across
the
entire
rare
disease
ecosystem
.

CDFD
AIIMS Delhi
TPG
BGCI
GHRC
Manovikas
SGRH
CDFD
AIIMS Delhi
TPG
BGCI
GHRC
Manovikas
SGRH

Built for Trust. Designed for Healthcare.

Enterprise-grade security, privacy, and compliance built into every layer of the platform.

  1. 1Your institution retains full ownership and control of its data.
  2. 2Access is restricted based on user roles and responsibilities.
  3. 3Every action is securely logged for complete traceability.
  4. 4Data is protected through encryption in transit and at rest.
  5. 5Hosted on enterprise-grade infrastructure with continuous monitoring.

Solutions for Every Stakeholder in the Rare Disease Ecosystem

Purpose-built solutions for every organization involved in rare disease care.

Problem

Managing complex genetic cases with fragmented records, extensive documentation, and limited clinical support.

Solution

AI-assisted workflows, structured clinical data capture, and integrated decision support designed specifically for rare disease care.

Supporting the Entire Rare Disease Journey

From first symptoms to long-term care, Genetico helps connect every stage of the patient journey.

Problem

Years of Diagnostic Delay

Patients often experience years of diagnostic delays due to limited awareness, fragmented information, and complex referral pathways.

Solution

Structured, Connected Pathways

Structured patient journeys, AI-assisted clinical workflows, and connected referral pathways that support earlier diagnosis and access to care.

FAQs

Frequently Asked Questions

Answers to common questions about Genetico, IndiGeneUs.AI, and how we support rare and genetic disease care.

  • Genetico is building the digital backbone for the rare and genetic disease ecosystem. By connecting clinical care, research, public health, and AI, we transform fragmented healthcare data into structured, interoperable, and actionable intelligence.

  • IndiGeneUs.AI is Genetico's AI-enabled clinical genetics platform. It supports structured phenotype capture, pedigree analysis, clinical decision support, longitudinal patient management, and research workflows through a unified digital ecosystem.

  • Genetico is designed for clinicians, hospitals, diagnostic laboratories, research institutions, biotechnology organizations, and public health programs working in rare and genetic diseases.

  • Yes. IndiGeneUs.AI is designed to integrate with existing healthcare infrastructure, including hospital and laboratory information systems, enabling organizations to strengthen their clinical genetics workflows without disrupting existing operations.

  • Rare disease data often exists in fragmented reports, PDFs, and free-text clinical notes. Structured data enables better clinical decision-making, AI-assisted analysis, longitudinal patient management, research, and public health initiatives. It forms the foundation for a connected rare disease ecosystem.

Building the Future of Rare Disease Intelligence Together

Discover how AI-enabled workflows, clinical decision support, and structured data infrastructure can help advance rare disease care, research, and public health initiatives.

We'll connect you to our medical team to walk through workflows, integration and a 2-week pilot at your center.

By submitting, you agree to be contacted by Genetico. We never share your information with third parties.