Sat, Oct 17, 2026 | Updated 01:28 IST
Genetidoc Launches India's First Online Forum for Rare Genetic Diseases
Oct 09, 2026
Thiruvananthapuram (Kerala) [India], October 9: Genetidoc Genetic Clinic and DNA Testing Lab has launched the Genetidoc Rare Disease Forum. It is India's first online...
Gujarat-Based Biobank powers India's fight against rare diseases
Mar 25, 2026
In a significant step towards tackling rare genetic disorders, a Gujarat-based institute has established India's first national biobank dedicated to rare Lysosomal Storage Disorders...
Kejriwal visits family of boy suffering from rare genetic disease
Sep 12, 2023
Delhi Chief Minister Arvind Kejriwal on Tuesday met 18-month-old toddler Kanav, who is suffering from a rare genetic disease, at his house in Najafgarh.
Venkaiah Naidu inaugurates Pediatric Rare Genetic Disorders Laboratory in Hyderabad
Feb 20, 2021
Hyderabad (Telangana) [India], February 20 : Vice President M Venkaiah Naidu inaugurated the 'Pediatric Rare Genetic Disorders Laboratory' on the Silver Jubilee of the...
True Hope Foundation extends RS. 1.21 Crore support to Indore's Anika Sharma in her fight against SMA Type 2
Jun 18, 2026
In a significant step toward supporting children affected by rare diseases, Jodhpur-based True Hope Foundation has extended financial assistance of ₹1.21 crore for the...
Delhi couple resorts to crowdfunding for treatment of their infant suffering from rare genetic disorder
Mar 05, 2021
New Delhi [India], March 6 : A couple living in Delhi's Paschim Vihar are trying to raise Rs 16 crore through crowdfunding to save...
The Avestagenome Project® and TIGS Sign Strategic Alliance to Advance Research in Rare Genetic Disorders
Feb 24, 2025
Pakistan's classic trait of denying persecution of minorities
Dec 22, 2022
Using the strength In Unified Purpose, Big Eyes Coin is about to make over 100x gain more than Polkadot and Zcash
Dec 15, 2022
Indo-Irish Biotech startup CyGenica secures funding from SOSV to accelerate cancer and rare genetic disease therapy
Jun 08, 2021
Plea moved in Delhi HC seeking immediate release of rare disease funds for 3-year-old girl's life-saving bone marrow transplant
Jun 02, 2026
Delhi HC seeks Centre's response on plea seeking ₹40 lakh rare disease funding for 3-year-old girl's bone marrow transplant
Jun 06, 2026
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