# |
Rank |
Epic Display Name |
Cerner Name |
Cerner PDM |
Informatics Workgroup |
1. |
99989 |
Factor 5 leiden
|
HLX Factor V Leiden CASE |
5160174 |
Molpath inhouse |
2. |
99989 |
Hemochromatosis (HFE) Mutation Molecular Detection
|
HLX HEMOCHROMATOSIS CASE |
5160990 |
Molpath inhouse |
3. |
99989 |
Prothrombin (PTR) Mutation Molecular Detection
|
xMGPTR |
5160177 |
Molpath inhouse |
4. |
99989 |
Quantitative BCR/ABL Molecular Detection
|
HLX BCR-ABL by RT-PCR CASE |
5911120 |
Molpath inhouse |
5. |
99989 |
Quantitative JAK2 V617F Molecular Detection
|
HLX JAK-2 Mutation CASE |
5160105 |
Molpath inhouse |
6. |
99989 |
MTHFR Mutation Molecular Detection
|
HLX MTHFR CASE |
5160200 |
Molpath inhouse |
7. |
99989 |
Hereditary Inclusion Body Myopathy (HIBM) Mutation Molecular Detection
|
HLX HIBM CASE |
5157200 |
Molpath inhouse |
8. |
99989 |
Calreticulin (CALR) Mutation Molecular Detection
|
HLX CALR CASE |
1763033 |
Molpath inhouse |
9. |
99989 |
FLT3 ITD-TKD Mutation Molecular Detection
|
HLX FLT3 CASE |
1863168 |
Molpath inhouse |
10. |
99989 |
Spinal Muscular Atrophy (SMA) Molecular Detection
|
HLX Spinal Muscular Atrophy (SMA) Case |
5910160 |
Molpath inhouse |
11. |
99989 |
MPL Mutation Molecular Detection
|
HLX MPL Mutation Analysis Case |
1559701 |
Molpath inhouse |
12. |
99989 |
B Cell Gene Rearrangement (IGR) Molecular Detection
|
xMGIGR |
5160170 |
Molpath inhouse |
13. |
99989 |
T Cell Gene Rearrangement (TCR) Molecular Detection
|
xMGTCR |
5160176 |
Molpath inhouse |
14. |
99989 |
Fragile X Mutation (FMR1) Molecular Detection
|
HLX Fragile X CASE |
5160403 |
Molpath inhouse |
15. |
99989 |
HLA B57:01 Molecular Detection
|
HLX HLA Antigen B5701 Case |
228468 |
Molpath inhouse |
16. |
99989 |
HLA B27 Molecular Detection
|
HLX HLA B27 Genotype Case |
238466 |
Molpath inhouse |