MUMBAI, India, Nov. 2 -- Intellectual Property India has published a patent application (202511081818 A) filed by Genomiki Solutions Private Limited on September 28, 2025, for Genetic Screening Panel For Early Detection Of Rare, Treatable Neonatal-Onset Disorders.
Inventors include Dr. Deeksha Bhartiya; and Dr. Priyanshu Mathur.
The application for the patent was published on October 30, 2026, under issue no. 44/2026.
Abstract: A panel for neonatal genetic screening is disclosed herein. The panel comprises 503 genetic disorders relevant to a neonatal or early-infant population. The panel also 473 selected genes, each selected gene being mapped to at least one of the genetic disorders. The genetic disorders are selected based on rarity, monogenic genetic basis, neonatal or early-infant relevance, evidence of treatability, and clinical manageability. Each selected gene and the genetic disorder mapped thereto is associated with clinical information selected from inheritance information, age-of-onset information, treatability information, clinical manageability information, and supporting evidence.
Disclaimer: Curated by HT Syndication.
