| A | B | C | D | E | |
|---|---|---|---|---|---|
1 | |||||
2 | Birthdate | 03-Apr-2021 | <<< Enter Pt's Date of Birth here (dd-mmm-yyyy) | ||
3 | Affordable | No | |||
4 | High-Risk | Yes | |||
5 | Addon Charges (Rs) | 400 | Shipping & Collection Charges | ||
6 | |||||
7 | Age (Days) | 102 | |||
8 | |||||
9 | Available Panels | Price | Tests Included | ||
10 | >>> | FS+Hb+ (65) | NA | Fatty Acid Oxidation Disorders, Organic Acid Disorders, Amino Acid Disorders, Other Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6-Phosphate Dehydrogenase Deficiency, Biotinidase Deficiency, Cystic Fibrosis, Sickle Cell Anemia, Sickle-C Disease, S-βeta Thalassemia, Hb Variants | |
11 | FS+ (61) | NA | Fatty Acid Oxidation Disorders, Organic Acid Disorders, Amino Acid Disorders, Other Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6-Phosphate Dehydrogenase Deficiency, Biotinidase Deficiency, Cystic Fibrosis | ||
12 | FS (60) | 6400 | Fatty Acid Oxidation Disorders, Organic Acid Disorders, Amino Acid Disorders, Other Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6-Phosphate Dehydrogenase Deficiency, Biotinidase Deficiency | YES | |
13 | MS+BIO1 (56) | 5150 | Fatty Acid Oxidation Disorders, Organic Acid Disorders, Amino Acid Disorders, Other | YES | |
14 | MS (55) | 4650 | Fatty Acid Oxidation Disorders, Organic Acid Disorders, Amino Acid Disorders, Other | YES | |
15 | Bio7 (7) | NA | Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6-Phosphate Dehydrogenase Deficiency, Biotinidase Deficiency, Cystic Fibrosis, Phenylketonuria | ||
16 | Bio6 (6) | NA | Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6-Phosphate Dehydrogenase Deficiency, Biotinidase Deficiency, Cystic Fibrosis | ||
17 | Bio5 (5) | NA | Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6-Phosphate Dehydrogenase Deficiency, Biotinidase Deficiency | ||
18 | Bio4 (4) | NA | Congenital Hypothyroidism, Galactosemia, Congenital Adrenal Hyperplasia, Glucose-6-Phosphate Dehydrogenase Deficiency | ||
19 | >>> | MCGM (7) | NA | Congenital Hypothyroidism, Congenital Adrenal Hyperplasia, Glucose-6-Phosphate Dehydrogenase Deficiency, Sickle Cell Anemia, Sickle-C Disease, S-βeta Thalassemia, Hb Variants | |
20 | |||||