Join the Global Albinism Alliance community meeting in Delhi on May 4, 2026. Open to persons with albinism and families. Register now to attend.
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- Global Albinism Alliance to Host Community Meeting in Delhi on May 4
- IORD seeks seat on South East Asia rare disease task force panel
- Dr. Anil Kumar Mandal: 40-Year Journey Advancing Care in Congenital Glaucoma
- World Rare Disease Day 2026: Dr. Ramaiah Muthyala Focuses on Rare Ophthalmic Disorders
- India: Rare Ophthalmic Disorders Take Centrestage at World Rare Disease Day-2026
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IORD
Indian Organization For Rare Diseases
(IORD), a not-for-profit umbrella organization represents interests of all stakeholders of Rare Diseases in India including individual patients, patient support groups, health policy advocates and health care providers.
CONTACT US
Indian Organization For Rare Diseases
Registered Office (India):
Plot No. 397, Road No. 22B, Jubilee Hills, Hyderabad – 500033, Telangana, India.
Phone: +91-9666438880
Email: indiaord@gmail.com