| Test Code |
Test Name |
Location |
Methodology |
Disease Category |
MRP |
Days |
|
MGM107
|
Primary hyperoxaluria gene panel |
Bangalore |
Next Generation Sequencing |
Nephrology |
21700 |
21 |
|
MGM1071
|
MYH9 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1073
|
Hyper-immunoglobulin E syndrome (DOCK8 and STAT3) gene sequencing |
Bangalore |
Next Generation Sequencing |
Immunology |
21700 |
21 |
|
MGM1074
|
WAGR syndrome (PAX6 and WT1) gene sequencing |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
21700 |
21 |
|
MGM1075
|
Nail-patella syndrome (LMX1B) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1077
|
Dystonia-28 (KMT2B) gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-Movement Disorders |
21700 |
21 |
|
MGM1078
|
GATA1 and UROS gene sequencing |
Bangalore |
Next Generation Sequencing |
Hematology |
21700 |
21 |
|
MGM108
|
Xanthinuria gene panel |
Bangalore |
Next Generation Sequencing |
Nephrology |
21700 |
21 |
|
MGM109
|
Benign infantile epilepsy gene panel |
Bangalore |
Next Generation Sequencing |
Neurology-Epilepsy |
21700 |
21 |
|
MGM1118
|
KHDC3L and NALP7 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM112
|
Epileptic encephalopathy gene panel |
Bangalore |
Next Generation Sequencing |
Neurology-Epilepsy |
21700 |
21 |
|
MGM1120
|
Townes-Brocks syndrome (SALL1) gene sequencing |
Bangalore |
Next Generation Sequencing |
Skeletal dysplasia |
21700 |
21 |
|
MGM1121
|
GDF1 and PKD1L1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Cardiology |
21700 |
21 |
|
MGM113
|
Familial female mental retardation/epilepsy gene panel |
Bangalore |
Next Generation Sequencing |
Neurology-Epilepsy |
21700 |
21 |
|
MGM114
|
Progressive myoclonic epilepsy gene panel |
Bangalore |
Next Generation Sequencing |
Neurology-Epilepsy |
21700 |
21 |
|
|
|
|
