In an era where rare diseases affect 400 million people globally, PhenoTips isn't just building another pedigree maker—it's architecting the complete genomic health record. With a lean team of 29 and $2.8M in revenue, they're proving that specialized software can fundamentally transform how medical genomics departments operate.

"They're not just digitizing paper—they're creating the operating system for rare disease diagnosis."

The technology stack reveals a modern, pragmatic approach. They're using Tailwind CSS, Bootstrap, and Ant Design—tools that prioritize developer velocity over bleeding-edge innovation. This isn't a team chasing JavaScript framework trends; they're building reliable clinical software. The presence of Swiper and AOS (Animate On Scroll) suggests a polished, patient-facing interface that balances clinical rigor with user experience.

• Rare disease focus: Building for the 5% of cases where genomics matters most
• Clinical workflow integration: Not just data storage, but active diagnostic support
• Paper-free mandate: Targeting the 60% of genetics departments still using paper records
• Webinar-driven education: Using content to deepen existing user engagement, not acquire new ones