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View Palmetto Test Indicators for our Molecular Pathology

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View Palmetto Test Indicators for our Molecular Pathology Powered By Docstoc
					MML Test Code
1A2, 1A2O
2C19O, 2C19S
2C9S, 2C9SO
2D6, 2D6O
2D6T, 2D6TO
83361
83363
83365
83367
88955
88956
88957
89669
89670
89671
89672
88958
89045
ACVK
ADHP
AGPB
AGXKM
AGXMS
AGXT
AJP
AJPWO
AMYKM
AMYL
APCRV
APOB
APOE
ARPKD
ARPKM
BA190
BADX
BAKDM
BCGBM, BCGR, BCGRV
BCRAB
BLM
BRAF
BTDKM
BTDMS
BTKFP
BTKK
BTKMP
BTKS
CANW
CFPB
CFTRK
CFTRM
CGH
CHEP
COMT, COMTO
CSRKM
CSRMS
CYPKP
CYPSP
DISI
DRD3, DRD3O
DRD4, DRD4O
DRPLA
ENGK
F5DNA
FABKM
FABMS
FANCA
FAPKM
FAPMS
FBKM
FBN1
FBNN
FD
FECHK
FECHS
FIXKM
FIXMS
FXPB
GAAKM
GAAMS
GAL6
GALTK
GALTM
GAUW
GCT
GRNKM
GRNMS
HAEVP
HAPB
HBELC
HEXKM
HEXMS
HHEMO
HHTP
HL15O, HL15
HLA57, HLA57O
HNPCC
HP
HPKM
HTR2, HTR2O
HTT, HTTO
IVD
JAK2B, JAK2M, JAK2V
JAKXB, JAKXM
KBF,
KF, KFT
KITAS
LDLRK
LDLRS
MAHKM
MAHMS
MAPTK
MAPTM
MCADK
MCADP
MCC
MCDKM
MCDMS
MCIV
ME2KM
ME2MS
MENKM
MENMS
MEVP
MLBRF
MLH12
MLH1H
MLHKM
MLHMS
MPLB, MPLM
MSH2K
MSH2M
MSH6K
MSH6M
MSIO
MTHFR
MUGS
MYH
NAGR
NARC
NAT2, NAT2O
NITF, NITU
NPCKM
NPCMS
NPD
NPM1
OPRMO
PMLR
PT11
PT1K
PTNT
PTP22
PWDNA
REVP
SBMA
SCADK
SCADM
SDHDD
SDHKM
SDHSB
SDHSC
SDHSD
SDHSP
SPCID
TACIF
TACIG
TAP
TCGBM, TCGR, TCGRV
TGF1
TGF2
TGFK1
TGFK2
THEVP
THRMP
TSD
TTRX
U1A1
UGT2
UGTI
UGTK
UOSMF
UPD
VHLD
VHLKP
VHLSP
VLCKM
VLCMS
WARFO, WARFP
WDKM
WDMS
YMICR
ZYG
A1ATR
VWD2N
Test Description
Cytochrome P450 1A2 Genotype
Cytochrome P450 2C19 Genotype by Sequence Analysis
Cytochrome P450 2C9 Genotype by Sequence Analysis
Cytochrome P450 2D6 Genotype
Cytochrome P450 2D6 Genotype for Tamoxifen Hormonal Therapy
Synovial Sarcoma by Reverse Transcriptase PCR, Paraffin
Ewing Sarcoma/Primitive Neuroectodermal Tumors (ES/PNET) by Reverse Transcriptase PCR (RT-PCR), Paraffin
Desmoplastic Small Round Cell Tumor (DSRCT) by Reverse Transcriptase PCR (RT-PCR), Paraffin
Alveolar Rhabdomyosarcomas (ARMS) by Reverse Transcriptase PCR, Paraffin
KIT, Mutation Analysis, Exon 8
KIT, Mutation Analysis, Exon 13
KIT, Mutation Analysis, Exon 17
KIT, Mutation Analysis, Exon 9
KIT, Mutation Analysis, Exon 11
PDGFRA, Mutation Analysis, Exon 12
PDGFRA, Mutation Analysis, Exon 18
PDGFRA, Mutation Analysis, Exon 14
BRAF Mutation (T1799A) Analysis, Thyroid
Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene, Known Mutation
Familial Hypercholesterolemia/Autosomal Dominant Hypercholesterolemia Genetic Testing Reflex Panel
Alpha-Globin Gene Analysis
AGXT Gene, Known Mutation
AGXT Gene, Full Gene Analysis
Alanine:Glyoxylate Aminotransferase (AGXT) Mutation Analysis (G170R), Blood
Ashkenazi Jewish Mutation Analysis Panel With Cystic Fibrosis (CF)
Ashkenazi Jewish Mutation Analysis Panel Without Cystic Fibrosis (CF)
Amyloidosis, Transthyretin-Associated Familial, Known Mutation
Amyloidosis, Transthyretin-Associated Familial, DNA Sequence, Blood
Activated Protein C Resistance V (APCRV), with Reflex to FV Leiden, Plasma
Apolipoprotein B-100 Molecular Analysis, R3500Q and R3500W
Apolipoprotein E Genotyping, Blood
Autosomal Recessive Polycystic Kidney Disease (ARPKD), Full Gene Analysis
Autosomal Recessive Polycystic Kidney Disease (ARPKD), Known Mutation
BCR/ABL, p190, mRNA Detection, Reverse Transcription-PCR (RT-PCR), Quantitative, Monitoring Assay
BCR/ABL, mRNA Detection, Reverse Transcription-PCR (RT-PCR), Qualitative, Diagnostic Assay
BCR/ABL, Tyrosine Kinase Inhibitor Resistance, Kinase Domain Mutation Screen
Immunoglobulin Gene Rearrangement
BCR/ABL, p210, mRNA Detection, Reverse Transcription-PCR (RT-PCR), Quantitative, Monitoring Chronic Myelogenous Leuke
Bloom Syndrome, Mutation Analysis, 2281del6/ins7
BRAF Mutation Analysis (V600E), Tumor
Biotinidase Deficiency, BTD Gene, Known Mutation
Biotinidase Deficiency, BTD Full Gene Analysis
Bruton's Tyrosine Kinase (BTK) Genotype and Protein Analysis, Full Gene Sequence and Flow Cytometry
Bruton's Tyrosine Kinase (BTK) Genotype, Known Mutation
Bruton's Tyrosine Kinase (BTK) Genotype and Protein Analysis, Known Mutation Sequencing and Flow Cytometry
Bruton's Tyrosine Kinase (BTK) Genotype, Full Gene Sequence
Canavan Disease, Mutation Analysis, ASPA
Cystic Fibrosis Mutation Analysis, 106-Mutation Panel
CFTR Gene, Known Mutation
CFTR Gene, Full Gene Analysis
Array Comparative Genomic Hybridization (aCGH), Whole Genome, Constitutional
Chimerism-Recipient Engraftment (Post)
Catechol-O-Methyltransferase Genotype
Calcium Sensing Receptor (CASR) Gene, Known Mutation
Calcium Sensing Receptor (CASR) Gene, Mutation Screen
21-Hydroxylase Gene (CYP21A2), Known Mutation
21-Hydroxylase Gene (CYP21A2), Full Gene Analysis
HLA Class I Molecular Typing Disease Association
Dopamine Receptor D3 Genotype
Dopamine Receptor D4 Genotype (DRD4), Blood
Dentatorubral-Pallidoluysian Atrophy (DRPLA) Gene Analysis
Hereditary Hemorrhagic Telangiectasia, ENG Gene, Known Mutation
Factor V Leiden (R506Q) Mutation, Blood
Fabry Disease, Known Mutation
Fabry Disease, Full Gene Analysis
Fanconi Anemia C Mutation Analysis, IVS4(+4)A->T and 322delG
Familial Adenomatous Polyposis (FAP) Known Mutation
Familial Adenomatous Polyposis (FAP) Mutation Screen
FBN1 Genetic Analysis, Known Mutation
FBN1, Full Gene Sequence
FBN1, Partial Gene Sequence, Neonatal Marfan Syndrome
Familial Dysautonomia, Mutation Analysis, IVS20(+6T->C) and R696P
Ferrochelatase (FECH) Gene, Known Mutation
Ferrochelatase (FECH) Gene, Full Gene Analysis
Hemophilia B, Factor IX Gene Known Mutation Screening
Hemophilia B, Factor IX Gene Mutation Screening
Fragile X Syndrome, Molecular Analysis
Pompe Disease, Known Mutation
Pompe Disease, Full Gene Sequencing
Galactosemia Gene Analysis (6-Mutation Panel)
Galactosemia Gene Analysis, Known Mutation
GALT Gene, Full Gene Analysis
Gaucher Disease, Mutation Analysis, GBA
Galactosemia Reflex, Blood
Progranulin Gene (GRN), Known Mutation
Progranulin Gene (GRN), Full Gene Analysis
Hemolytic Anemia Evaluation
Hemophilia A, Molecular Analysis for Inversion, Diagnosis and Carrier Detection
Hemoglobin Electrophoresis Cascade, Blood
Tay-Sachs Disease, HEXA Gene, Known Mutation
Tay-Sachs Disease, HEXA Gene, Full Gene Analysis
Hemochromatosis HFE Gene Analysis, Blood
Hereditary Hemorrhagic Telangiectasia, ENG and ACVRL1 Full Gene Analysis
HLA-B 1502 Genotype, Carbamazepine Hypersensitivity
HLA-B 5701 Genotype, Abacavir Hypersensitivity
Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Screen
Hereditary Pancreatitis, Mutation Screen
Hereditary Pancreatitis, Known Mutation
Serotonin Receptor Genotype (HTR2A and HTR2C)
Serotonin Transporter Genotype, Blood
Isovaleryl-CoA Dehydrogenase (IVD) Mutation Analysis (A282V)
JAK2 V617F Mutation Detection
JAK2 Exon 12 and Other Non-V617F Mutation Detection
POTASSIUM, BODY FLUID
POTASSIUM, FECES
KIT Asp816Val Mutation Analysis, Qualitative PCR
Familial Hypercholesterolemia, LDLR Gene, Known Mutation
Familial Hypercholesterolemia, LDLR Full Gene Sequencing
Methylmalonic Aciduria and Homocystinuria, cblC Type, Known Mutation
Methylmalonic Aciduria and Homocystinuria, cblC Type, Full Gene Analysis
MAPT Gene, Sequence Analysis, Known Mutation
MAPT Gene, Sequence Analysis, 7 Exon Screening Panel
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency, Known Mutation
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency Molecular Profile
Maternal Cell Contamination, Molecular Analysis
MLYCD Gene, Known Mutation
MLYCD Gene, Full Gene Analysis
Mucolipidosis IV, Mutation Analysis, IVS3(-2)A->G and del6.4kb
MECP2 Gene, Known Mutation
MECP2 Gene, Full Gene Analysis
Multiple Endocrine Neoplasia Type 2 (2A, 2B, FMTC) Known Mutation
Multiple Endocrine Neoplasia Type 2 (2A, 2B, FMTC) Mutation Screen
Methemoglobinemia Evaluation
MLH1 Hypermethylation and BRAF Mutation Analyses, Tumor
MLH1/MSH2 Mutation Screen
MLH1 Hypermethylation Analysis, Tumor
MLH1 Known Mutation
MLH1 Mutation Screen
MPL Exon 10 Mutation Detection, Blood
MSH2 Known Mutation
MSH2 Mutation Screen
MSH6 Known Mutation
MSH6 Mutation Screen, Blood
Microsatellite Instability (MSI), Tumor
5,10-Methylenetetrahydrofolate Reductase, Mutation, Blood
Hexosaminidase A (MUGS), Serum
MYH Gene Analysis for Multiple Adenoma, Y165C and G382D
Hexosaminidase A and Total, Leukocytes/Molecular Reflex
Narcolepsy Associated Antigen, Blood
N-Acetyltransferase 2 Gene (NAT2), Full Gene Sequence
NITROGEN, TOTAL
Niemann-Pick Type C Disease, Known Mutation
Niemann-Pick Type C, Full Gene Analysis
Niemann-Pick Disease, Types A and B, Mutation Analysis
Nucleophosmin (NPM1) Mutation Analysis
Opioid Receptor, Mu 1 (OPRM1) Genotype for Naltrexone Efficacy, Saliva
PML/RARA Quantitative, PCR
PTPN11, Full Gene Sequence, Blood
PTPN11 Gene, Known Mutation, Blood
Prothrombin G20210A Mutation, Blood
PTPN22 Genotype, 1858C->T
Prader-Willi/Angelman Syndrome, Molecular Analysis
Erythrocytosis Evaluation
Spinobulbar Muscular Atrophy (Kennedy's Disease), Molecular Analysis
Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Known Mutation
Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Mutation Screen
Succinate Dehydrogenase (SDH) Gene, Deletion Detection
Succinate Dehydrogenase (SDH) Gene, Known Mutation
Succinate Dehydrogenase (SDH) Subunit B Gene Analysis
Succinate Dehydrogenase (SDH) Subunit C Gene Analysis
Succinate Dehydrogenase (SDH) Subunit D Gene Analysis
Succinate Dehydrogenase (SDH) Gene Analysis
Specimen Source Identification
Transmembrane Activator and CAML Interactor (TACI) Gene, Full Gene Analysis
Transmembrane Activator and CAML Interactor (TACI) Gene, Known Mutation Analysis
Thymopoiesis Assessment Profile
T-Cell Receptor Gene Rearrangement, PCR
TGFBR1, Full Gene Sequence
TGFBR2, Full Gene Sequence
TGFBR1 Gene, Known Mutation
TGFBR2 Gene, Known Mutation
Thalassemia and Hemoglobinopathy Evaluation
Thrombophilia Profile
Tay-Sachs Disease, Mutation Analysis, HEXA
Amyloidosis, Transthyretin-Associated Familial, Reflex, Blood
UDP-Glucuronosyl Transferase 1A1 TA Repeat Genotype, UGT1A1
UDP-Glucuronosyl Transferase 1A1 (UGT1A1), Full Gene Sequencing, Hyperbilirubinemia
UDP-Glucuronosyl Transferase 1A1 (UGT1A1), Full Gene Sequencing, Irinotecan Hypersensitivity
UDP-Glucuronosyl Transferase 1A1 (UGT1A1) Gene, Known Mutation
Osmolality, Feces
Uniparental Disomy
Von Hippel-Lindau (VHL) Deletion Detection
Von Hippel-Lindau (VHL) Gene, Known Mutation
Von Hippel-Lindau (VHL) Gene, Full Gene Analysis
Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Known Mutation
Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Full Gene Analysis
Warfarin Sensitivity Genotype by Sequence Analysis
Wilson Disease Known Mutation, ATP7B DNA Sequencing
Wilson Disease Mutation Screen, ATP7B DNA Sequencing
Y Chromosome Microdeletions, Molecular Detection
Zygosity Testing (Multiple Births)
Alpha-1-Antitrypsin Deficiency Profile
von Willebrand Disease 2N (Normandy)
Palmetto Test Indicator (PTI)
PBM73
PBM74
PBM75
PBM76
PBM77
PBM00
PBM01
PBM02
PBM03
PBM04
PBM05
PBM06
PBM07
PBM08
PBM09
PBM10
PBM11
PBM78
PBM12
PBM13
PB440
PBM14
PBM15
PBM16
PBM17
PBM18
PBM19
PB640
PBM20
PBM21
PBM79
PBM22
PBM23
PBM80
PBM81
PBM82
PBM84
PBM83
PBM24
PBM85
PBM25
PBM26
PBM27
PBM28
PBM29
PBM30
PBM86
PBM87
PBM88
PBM89
PBM90
PBM91
PBM31
PBM32
PBM33
PBM34
PBM35
PBM92
PBM36
PBM37
PBM38
PBM39
PBM93
PBM94
PBM95
PBM96
PBM97
PBG45
PBM98
PBG02
PBM99
PBN00
PBM40
PBM41
PBN01
PBN02
PBN03
PBN04
PBN05
PBF81
PBN06
PBN07
PBN09
PBN08
PBM42
PBM43
PBN10
PBN11
PBN12
PBN13
PBN14
PBN15
PBM44
PBN16
PBN17
PBN18
PBG01
PBN19
PBM46
PBM47
PBM48
PBN20
PBN21
PBN22
PBN23
PBN24
PBN25
PBN26
PBM49
PBM50
PBM51
PBM52
PBN27
PBN28
PBN29
PBM53
PBM54
PBN30
PBN31
PBN32
PBN33
PBF97
PBN34
PBN35
PBN36
PBN37
PBN38
PBN39
PBN40
PBN41
PBN42
PBN43
PBN44
PBN45
PBN46
PBN47
PBG69
PBN82
PBN48
PBN49
PBL16
PBN50
PBN51
PBN52
PBN53
PBM55
PBN54
PBN55
PBN56
PBN57
PBN58
PBN59
PBN60
PBG68
PBM56
PBM57
PBM58
PBM59
PBM60
PBM61
PBM62
PBM63
PBN61
PBM64
PBM65
PBM66
PBN62
PBM67
PBM68
PBM69
PBM70
PBN63
PBN64
PBN65
PBN66
PBN67
PBN68
PBN69
PBN70
PBN71
PBN72
PBN73
PBN74
PBN75
PBM71
PBM72
PBN76
PBN77
PBG46
PBN78
PBN79
PBN80
PBN81

				
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posted:8/20/2012
language:Latin
pages:15