To Top
0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z


The information contained in the Organizational Database (ODB) is provided for informational purposes only. There is no implied endorsement by NORD. NORD does not promote or endorse participation in any specific organization. The information is subject to change without notice. Every effort is made to ensure that the details for each entry are as current as possible.

Organization for Rare Diseases India


#16/2, Sri Krishna Krupa, 19th Cross
8th Main, kashimutt Road
Malleshwaram, Bengaluru, Karnataka 560055 India

Email Address

[email protected]


ORDI is a national umbrella organization representing the collective voice of all patients with rare diseases in India. ORDI's objectives include public policy development/implementation to cover rare, undiagnosed and genetic diseases patients in India; accelerating diagnosis and treatment options for patients with rare diseases through public-private partnerships; advocating for mandatory newborn screening; representing India in international consortia such as IRDiRC, UDN, ICORD, etc.; and organizing national and international conferences to bring all stakeholders of rare diseases together for debates and discussions. Facebook: Twitter:

Please Note

The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.

NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.