FamGenix
FamGenix is a cloud-based family health history and pedigree platform that helps clinicians, genetic counselors, and patients assess hereditary disease risk, serving healthcare providers, EHR partners, and individual patients across the US, Canada, the EU/UK, and Australia.
- Company typePrivate
- Founded2019
- HeadquartersBoynton Beach, United States
- Headcount1–10
- GTM typeB2B
- OfferingSoftware
What FamGenix does
FamGenix, Inc. (legal entity FamHis, Inc., dba FamGenix; headquartered in Fargo, ND with prior offices in Boynton Beach and Delray Beach, FL) builds a cloud-based family health history and pedigree platform that helps clinicians and patients assess hereditary disease risk. The platform is deployed on AWS with regional data residency in the US, Canada, the EU/UK, and Australia/Asia-Pacific, and is HIPAA- and GDPR-compliant (SOC 2 Type 1 completed April 2026, Type 2 in progress). Core products include the Provider Portal (a pedigree chart maker with built-in medical ontology — HPO, OMIM, CHV, NCI, HGNC — and automated guideline-based identification of patients meeting NCCN/ACMG/ASBrS referral criteria), the Patient App (a free mobile/web family health history questionnaire in English, Spanish, French, German, and Dutch with the FamShare family data-sharing feature), the Clinicians Platform (enterprise tier with EHR integration and API), a White Label/Embedded integration offer, and a Risk Server API that sub-licenses validated cancer and cardiovascular risk models (BOADICEA v6, Tyrer-Cuzick v8, BayesMendel, Gail, Claus, QRISK3). The company sells through a hybrid GTM: direct enterprise field sales to healthcare systems and clinical genetics teams, OEM/embedded and white-label licensing to EHR and clinical platforms, and a freemium direct-to-consumer channel via the free patient app on iOS and Android. Revenue is generated through individual subscriptions ($500/year per license), tiered enterprise contracts, and add-on fees for advanced risk models, custom questionnaires, EHR integration, and API access. Distribution is supported by partnerships with My Gene Counsel (March 2025) and Spesana (December 2023), and customer logos include City of Hope, UCSF, Boston Children's, Sharp HealthCare, Allina Health, UnityPoint Health, MercyOne, NHS Liverpool, and Cork University Hospital.
FamGenix firmographics
Firmographics- Name
- FamGenix
- Legal name
- FamHis, Inc.
- Website
- https://famgenix.com
- Company type
- Private
- Founded year
- 2019
- Operating status
- Operating
- Headcount range
- 1–10 employees
- Short description
- FamGenix is a cloud-based family health history and pedigree platform that helps clinicians, genetic counselors, and patients assess hereditary disease risk, serving healthcare providers, EHR partners, and individual patients across the US, Canada, the EU/UK, and Australia.
- Ownership category
- akta.pro rank
Where FamGenix is headquartered
LocationHeadquarters
- HQ city
- Boynton Beach
- HQ country
- United States
- HQ region
- North America
Offices7 records
Markets served
FamGenix business model
Business model- GTM type
- B2B
- Offering type
- Software
- Cost components
- Personnel, Technology or R&D, Infrastructure, Marketing or Sales, Operations, Others
Revenue model
- Individual Subscription License: Annual subscription license at $500/year for single-user access with unlimited pedigrees. Includes basic features with additional fees for premium add-ons like advanced risk models and patient questionnaires.
- Premium Enterprise License: Tiered pricing model for multi-user enterprise deployments with full feature access including multi-user access, EHR integration, API access, and custom branding. Additional fees apply for custom features.
- Risk Model Licensing (Add-on): Additional fee add-ons for individual risk assessment models: BOADICEA (+$100), Tyrer-Cuzick v8 (+$100), BayesMendel (+$100). Gail and Claus models included in base Individual license.
- Patient Questionnaire Add-on: Additional fee for standard or custom patient questionnaires and surveys. Standard questionnaires available as additional fee on Individual tier; custom data fields, questionnaires and surveys available as additional fee on both tiers.
- White-Label/Embedded Integration Licensing: Embedding FamGenix pedigree and risk assessment functionality into existing clinical systems with flexible licensing based on specific needs. Includes SSO integration and maintains patient data control within existing systems.
- API Risk Model Sub-licensing: Send family history data to FamGenix risk server via API to calculate and return results for display in customer's existing system. Enables risk model usage without full platform deployment.
- Free Patient App: Free mobile and web app for patients to record and maintain family health history, assess hereditary disease risk, and share with family members. Revenue generated from healthcare provider licensing of the platform that connects to patient data.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| Subscription | Annual | Individual license for single users at $500/yr with unlimited pedigrees |
| Subscription | Annual | Premium enterprise tier with tiered pricing for multi-user access and full integration capabilities |
Go-to-market motion3 records
Distribution channels4 records
Marketing channels6 records
FamGenix product offering
Product offeringCore offering
FamGenix provides a cloud-based family health history platform combining a pedigree drawing tool, integrated cancer and cardiovascular genetic risk assessment models, and a patient-facing mobile/web app. The platform enables clinicians, genetic counselors, and health systems to capture family health history, generate pedigrees, run multiple risk models simultaneously, and automatically identify patients meeting NCCN/ACMG referral criteria. It is offered through Individual subscriptions, Premium enterprise licenses, white-label/embedded OEM integrations, and a Risk Server API for existing clinical systems.
Product overview
FamGenix offers a unified family health history platform with three core components: the Provider Portal (a comprehensive pedigree drawing and genetic risk assessment tool for clinicians), the Patient App (a mobile/web application for family health history collection available in English, Spanish, French, German, and Dutch), and the Clinicians Platform (an enterprise solution combining all tools with EHR integration and API access). The platform integrates multiple cancer and cardiovascular risk assessment models (BOADICEA, Tyrer-Cuzick, BayesMendel, Gail, Claus, QRISK3) that run simultaneously to calculate 5-year, 10-year, and lifetime hereditary disease risk. The system automatically identifies patients meeting NCCN/ACMG clinical guidelines for genetic counseling referral. White-label and API options enable integration into existing clinical systems and custom branded deployments.
Differentiator
Problem solved
Functional benefit
Quantifiable outcome
- Patients meeting referral criteria are automatically identified based on NCCN/ACMG/ASBrS guidelines, displaying specific reasons criteria was met
- +3 more outcomes
Companies that use FamGenix
Customer profileNamed customers16 records
Segments3 records
Ideal customer profiles3 records
FamGenix technology and API
TechnologyAPI detail
- Has API
- Yes
- API docs
- API detail
Core technology
AI maturity
App detail
AI capability3 records
Feature7 records
FamGenix partnerships and signals
Strategic signalPartnerships
Three partnerships are on record, tiered core.
- My Gene CounselcoreStrategic partnership announced March 18, 2025 to provide healthcare centers with comprehensive digital genetic risk assessment and education toolkit. Combined platform facilitates risk assessment for hereditary cancer, cardiovascular disease, kidney disease, lymphoma, reproductive disorders, rare diseases, and other genetic conditions. Includes pre-test and post-test genetic education and ongoing dynamic updates specific to genetic test results.
- SpesanacoreStrategic partnership announced December 18, 2023 to advance precision medicine and integrate FamGenix hereditary risk screening with Spesana's clinical workflow ecosystem. FamGenix pedigree and hereditary risk assessment solutions planned to be seamlessly integrated with Spesana's solution, providing comprehensive tools for clinicians at point of care. Both companies committed to making family health histories part of every patient's electronic health record.
- Amazon Web Services (AWS)coreCloud infrastructure provider using AWS with dedicated regional servers in US, Canada, EU, UK, and Australia. AWS core infrastructure designed to meet most stringent security requirements for healthcare, banks, and military. Enables FamGenix to achieve and monitor HIPAA and GDPR compliance. Most extensive global network of regions ensures consistent security and compliance standards across all deployments.
Scale indicators5 records
Recent moves9 records
Expansion highlights6 records
FamGenix competitors and assessment
Company assessmentMarket position
Strengths5 records
Weaknesses5 records
Competitive moat6 records
Customer concentration
FamGenix social profiles
Digital presenceFamGenix compliance and trust
Trust signalCompliance3 records
FamGenix financial estimates
Financial estimateRevenue estimate
Valuation estimate
FamGenix leadership team
Management profileNumber of profiles
FamGenix funding detail
Funding detailFunding overview
Funding rounds4 records
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
FamGenix M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about FamGenix
What does FamGenix do?
FamGenix provides a cloud-based family health history platform combining a pedigree drawing tool, integrated cancer and cardiovascular genetic risk assessment models, and a patient-facing mobile/web app. The platform enables clinicians, genetic counselors, and health systems to capture family health history, generate pedigrees, run multiple risk models simultaneously, and automatically identify patients meeting NCCN/ACMG referral criteria. It is offered through Individual subscriptions, Premium enterprise licenses, white-label/embedded OEM integrations, and a Risk Server API for existing clinical systems.
Is FamGenix a public or private company?
FamGenix is a private company. It is classified as founder individual operated bootstrapped and is currently operating.
When was FamGenix founded?
FamGenix was founded in 2019. It employs 1 to 10 people.
Where is FamGenix based?
FamGenix is headquartered in Boynton Beach, United States, in the North America region.
How does FamGenix make money?
Seven revenue lines are on record. Individual Subscription License is the primary driver. The others are premium Enterprise License, risk Model Licensing (Add-on), patient Questionnaire Add-on, white-Label/Embedded Integration Licensing, API Risk Model Sub-licensing and free Patient App.
Does FamGenix have an API?
Yes. FamGenix offers API access for exchanging data to and from existing clinical systems. The Risk Server API allows external systems to pass patient family health history data and receive back genetic risk calculation results for display in their own system. API access is included with Premium/Premium tier licensing; Individual tier offers API access for an additional fee.