| PANELS | DESCRIPTION | PRICE | PAYMENT METHOD | 
|---|---|---|---|
| Hb+FS+ | Hb+FS+ is a comprehensive Newborn screening test that screens for over 65 TREATABLE disorders. The panel includes Fatty Acid Oxidation Disorders, Organic Acid Disorders, Amino Acid Disorders, Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6-Phosphate Dehydrogenase Deficiency, Biotinidase Deficiency, Cystic Fibrosis and Hemoglobinopathies. | ₹8,000 | Scan QR code or use UPI ID 9900655115@hdfcbank  | 
| FS | The FS test screens over 60 TREATABLE disorders that include Fatty Acid Oxidation Disorders, Organic Acid Disorders, Amino Acid Disorders, Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6-Phosphate Dehydrogenase Deficiency and Biotinidase Deficiency. | ₹7,250 | Scan QR code or use UPI ID 9900655115@hdfcbank  | 
| MS | MS screens for 55 TREATABLE disorders including Fatty Acid Oxidation Disorders, Organic Acid Disorders and Amino Acid Disorders. | ₹5,250 | Scan QR code or use UPI ID 9900655115@hdfcbank  | 
| BIO-6 | BIO6 screens 6 TREATABLE disorders including Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6 Phosphate Dehydrogenase Deficiency, Biotinidase Deficiency and Cystic Fibrosis. | ₹2,750 | Scan QR code or use UPI ID 9900655115@hdfcbank  | 
| BIO-5 | BIO5 screens 5 TREATABLE disorders including Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6 Phosphate Dehydrogenase Deficiency and Biotinidase Deficiency. | ₹2,400 | Scan QR code or use UPI ID 9900655115@hdfcbank  | 
| SMA | Spinal Muscular Atrophy or SMA is a genetic disease affecting the central nervous system, peripheral nervous system, and voluntary muscle movement (skeletal muscle). SMA is muscular because its primary effect is on muscles, which don’t receive signals from these nerve cells. Atrophy is the medical term for getting smaller, which is what generally happens to muscles when they’re not stimulated by nerve cells. Newborn Screening (NBS) can help detect SMA within the first week of life, before the onset of symptoms (usually within the first 6 months). | ₹2,500 | Scan QR code or use UPI ID 9900655115@hdfcbank  | 
| CUSTOM | If you wish to buy a test that isn’t listed, you can custom order your panel of interest here | Min ₹600 | Scan QR code or use UPI ID 9900655115@hdfcbank  |