# OpenAI o3 助力罕见遗传病诊断

- 来源：Greg Brockman (@gdb)
- 发布时间：2026-06-20 01:01
- AIHOT 分数：45
- AIHOT 链接：https://aihot.virxact.com/items/cmql76lts003qsl2scrwzfrgh
- 原文链接：https://x.com/gdb/status/2068016345451831480

## AI 摘要

Greg Brockman 发推介绍 OpenAI 与波士顿儿童医院合作，利用 o3 Deep Research 辅助诊断儿童罕见遗传病，相关成果发表在 NEJM AI。o3 模型虽已发布超过一年，Brockman 感慨如今模型的能力或将带来更大突破。

## 正文

OpenAI for helping families facing rare genetic diseases. This was done with o3 which is over a year old， amazing to think what will be possible with today's models.

### 引用推文

> OpenAI Newsroom：For families facing rare genetic diseases, answers can be hard to find. @HallieJackson spoke live with @_perloj and Dr. Catherine Brownstein about the new NEJM ...