查找地点
有关时间、上门服务和预约查找地点
有关时间、上门服务和预约This test includes the following genes: AAAS, ABCA12, ABCA3, ABCB11, ABCB4, ABCC8, ABCD1, ABCD4, ACAD9, ACADM, ACADSB, ACADVL, ACAT1, ACOX1, ACSF3, ADA, ADAMTS2, ADGRG1, ADGRV1, AGA, AGL, AGPAT2, AGPS, AGXT, AHI1, AICDA, AIPL1, AIRE, AK2, ALDH3A2, ALDH7A1, ALDOB, ALG1, ALG6, ALMS1, ALOX12B, ALOXE3, ALPL, AMPD2, AMT, ANO10, ANTXR2, AP3B1, ARG1, ARL13B, ARL6, ARSA, ARSB, ARX, ASL, ASNS, ASPA, ASS1, ATM, ATP13A2, ATP6V0A2, ATP6V0A4, ATP6V1B1, ATP6V1E1, ATP7A, ATP7B, ATP8B1, ATRX, AVPR2, B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCHE, BCKDHA, BCKDHB, BCS1L, BLM, BLOC1S3, BLOC1S6, BMP1, BRIP1, BSND, BTD, BTK, C19orf12, CAD, CAPN3, CAVIN1, CBS, CC2D2A, CCDC8, CCDC88C, CCN6, CD247, CD3D, CD3E, CD3G, CD40, CD40LG, CD8A, CDCA7, CDH23, CEP104, CEP290, CERKL, CERS3, CFTR, CHAT, CHMP1A, CHRNE, CHRNG, CHST6, CIB2, CIITA, CLCF1, CLCN1, CLCN5, CLN3, CLN5, CLN6, CLN8, CLP1, CLRN1, CNGA1, CNGB1, CNGB3, CNTNAP2, COASY, COL4A3, COL4A4, COL4A5, COL7A1, COLQ, CORO1A, CP, CPLANE1, CPS1, CPT1A, CPT2, CRLF1, CRTAP, CTC1, CTNS, CTSA, CTSD, CTSF, CTSK, CUL7, CWC27, CYBA, CYBB, CYP11A1, CYP11B1, CYP17A1, CYP1B1, CYP21A2, CYP27A1, CYP27B1, CYP4F22, CYP7B1, DBT, DCAF17, DCLRE1C, DDB2, DDC, DHCR7, DHDDS, DLD, DMD, DNMT3B, DOCK8, DOK7, DPYD, DTNBP1, DYNC2H1, DYSF, EDA, EFEMP2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, ELP1, EMD, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERCC8, ESCO2, ETFA, ETFB, ETFDH, ETHE1, EVC2, EXOSC3, EYS, F9, FA2H, FAH, FAM161A, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FBXL4, FHL1, FKBP10, FKRP, FKTN, FMO3, FMR1, FOXN1, FOXP3, FOXRED1, FRAS1, FREM2, FUCA1, G6PC1, GAA, GALC, GALE, GALK1, GALNS, GALT, GAMT, GATM, GBA1 (previously known as GBA), GBE1, GCDH, GFM1, GFPT1, GJB2, GLA, GLB1, GLDC, GLE1, GNE, GNPAT, GNPTAB, GNPTG, GNS, GPHN, GRHPR, GRIP1, GSS, GUSB, HADHA, HADHB, HAMP, HAX1, HBA1, HBA2, HBB, HCFC1, HELLS, HEXA, HEXB, HGSNAT, HINT1, HJV, HLCS, HMGCL, HOGA1, HPD, HPS1, HPS3, HPS4, HPS5, HPS6, HSD17B10, HSD17B4, HSD3B2, HYAL1, HYCC1 (previously known as FAM126A), HYLS1, IDS, IDUA, IFT140, IKBKB, IL2RA, IL2RG, IL7R, INPP5E, ITPA, IVD, JAK3, KCNJ1, KCTD7, KIF14, L1CAM, LAMA2, LAMA3, LAMB3, LAMC2, LAMP2, LARS1, LCA5, LCK, LHX3, LIFR, LIG4, LIPA, LIPN, LMBRD1, LOXHD1, LPL, LRAT, LRP2, LRPPRC, LTBP4, LYST, MAK, MALT1, MAN2B1, MANBA, MCCC1, MCCC2, MCEE, MCOLN1, MCPH1, MED17, MEFV, MESP2, MFSD8, MID1, MKKS, MKS1, MLC1, MMAA, MMAB, MMACHC, MMADHC, MMUT, MOCS1, MOCS2, MPI, MPL, MPV17, MTHFD1, MTM1, MTRR, MTTP, MVK, MYO7A, NAGA, NAGLU, NAGS, NBAS, NBN, NCF2, NCF4, NDUFAF2, NDUFAF5, NDUFS4, NDUFS6, NDUFS7, NDUFV1, NEB, NEU1, NGLY1, NHEJ1, NIPAL4, NONO, NPC1, NPC2, NPHP1, NPHP3, NPHS1, NPHS2, NR0B1, NTRK1, OAT, OBSL1, OCA2, OCRL, OPA3, OSTM1, OTC, OTOF, P3H1, PAH, PANK2, PC, PCBD1, PCCA, PCCB, PCDH15, PDHA1, PDHB, PDHX, PDP1, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PFKM, PGM3, PHGDH, PHKA1, PHKA2, PHKB, PHKG2, PKHD1, PLA2G6, PLEKHG5, PLOD2, PLP1, PMM2, PNP, PNPLA1, PNPO, POLG, POLH, POMGNT1, POMT1, POMT2, POR, POU3F4, PPIB, PPT1, PRCD, PRDM5, PRF1, PRKDC, PROP1, PSAP, PTPRC, PTS, PUS1, PYCR1, PYGM, QDPR, RAB23, RAG1, RAG2, RAPSN, RARS2, RD3, RDH12, RFX5, RFXANK, RFXAP, RLBP1, RMRP, RNASEH2A, RNASEH2B, RNASEH2C, RP2, RPE65, RPGR, RPGRIP1, RPGRIP1L, RPS6KA3, RS1, SACS, SAMHD1, SCO2, SDCCAG8, SDR9C7, SELENON, SEPSECS, SERPINF1, SGCA, SGCB, SGCD, SGCG, SGSH, SKIC2 (previously known as SKIV2L), SKIC3 (previously known as TTC37), SLC12A1, SLC12A6, SLC16A2, SLC17A5, SLC19A3, SLC22A5, SLC25A13, SLC25A15, SLC25A20, SLC26A2, SLC26A4, SLC27A4, SLC2A10, SLC35A3, SLC37A4, SLC39A4, SLC46A1, SLC4A11, SLC6A8, SLC7A7, SMARCAL1, SMN1, SMPD1, SP110, SPATA7, SPG11, SPG21, STAR, STK4, STX11, STXBP2, SUMF1, SUOX, SURF1, SYNE4, TAT, TAFAZZIN, TCIRG1, TCTN1, TCTN2, TCTN3, TECPR2, TF, TGM1, TH, TK2, TMEM138, TMEM216, TMEM231, TMEM237, TMEM38B, TMEM67, TMEM70, TNFSF11, TNXB, TPP1, TRAPPC11, TRIM32, TRMU, TSEN2, TSEN34, TSEN54, TSFM, TTC7A, TTC8, TTPA, TULP1, TYMP, TYR, UNC13D, UNG, USH1C, USH1G, USH2A, VLDLR, VPS13A, VPS13B, VPS45, VPS53, VRK1, WAS, WHRN, WNT1, WRN, XPA, XPC, ZAP70, ZBTB24 and ZNF469.
This test includes the following genes: AAAS, ABCA12, ABCA3, ABCB11, ABCB4, ABCC8, ABCD1, ABCD4, ACAD9, ACADM, ACADSB, ACADVL, ACAT1, ACOX1, ACSF3, ADA, ADAMTS2, ADGRG1, ADGRV1, AGA, AGL, AGPAT2, AGPS, AGXT, AHI1, AICDA, AIPL1, AIRE, AK2, ALDH3A2, ALDH7A1, ALDOB, ALG1, ALG6, ALMS1, ALOX12B, ALOXE3, ALPL, AMPD2, AMT, ANO10, ANTXR2, AP3B1, ARG1, ARL13B, ARL6, ARSA, ARSB, ARX, ASL, ASNS, ASPA, ASS1, ATM, ATP13A2, ATP6V0A2, ATP6V0A4, ATP6V1B1, ATP6V1E1, ATP7A, ATP7B, ATP8B1, ATRX, AVPR2, B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCHE, BCKDHA, BCKDHB, BCS1L, BLM, BLOC1S3, BLOC1S6, BMP1, BRIP1, BSND, BTD, BTK, C19orf12, CAD, CAPN3, CAVIN1, CBS, CC2D2A, CCDC8, CCDC88C, CCN6, CD247, CD3D, CD3E, CD3G, CD40, CD40LG, CD8A, CDCA7, CDH23, CEP104, CEP290, CERKL, CERS3, CFTR, CHAT, CHMP1A, CHRNE, CHRNG, CHST6, CIB2, CIITA, CLCF1, CLCN1, CLCN5, CLN3, CLN5, CLN6, CLN8, CLP1, CLRN1, CNGA1, CNGB1, CNGB3, CNTNAP2, COASY, COL4A3, COL4A4, COL4A5, COL7A1, COLQ, CORO1A, CP, CPLANE1, CPS1, CPT1A, CPT2, CRLF1, CRTAP, CTC1, CTNS, CTSA, CTSD, CTSF, CTSK, CUL7, CWC27, CYBA, CYBB, CYP11A1, CYP11B1, CYP17A1, CYP1B1, CYP21A2, CYP27A1, CYP27B1, CYP4F22, CYP7B1, DBT, DCAF17, DCLRE1C, DDB2, DDC, DHCR7, DHDDS, DLD, DMD, DNMT3B, DOCK8, DOK7, DPYD, DTNBP1, DYNC2H1, DYSF, EDA, EFEMP2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, ELP1, EMD, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERCC8, ESCO2, ETFA, ETFB, ETFDH, ETHE1, EVC2, EXOSC3, EYS, F9, FA2H, FAH, FAM1 |
This test includes the following genes: AAAS, ABCA12, ABCA3, ABCB11, ABCB4, ABCC8, ABCD1, ABCD4, ACAD9, ACADM, ACADSB, ACADVL, ACAT1, ACOX1, ACSF3, ADA, ADAMTS2, ADGRG1, ADGRV1, AGA, AGL, AGPAT2, AGPS, AGXT, AHI1, AICDA, AIPL1, AIRE, AK2, ALDH3A2, ALDH7A1, ALDOB, ALG1, ALG6, ALMS1, ALOX12B, ALOXE3, ALPL, AMPD2, AMT, ANO10, ANTXR2, AP3B1, ARG1, ARL13B, ARL6, ARSA, ARSB, ARX, ASL, ASNS, ASPA, ASS1, ATM, ATP13A2, ATP6V0A2, ATP6V0A4, ATP6V1B1, ATP6V1E1, ATP7A, ATP7B, ATP8B1, ATRX, AVPR2, B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCHE, BCKDHA, BCKDHB, BCS1L, BLM, BLOC1S3, BLOC1S6, BMP1, BRIP1, BSND, BTD, BTK, C19orf12, CAD, CAPN3, CAVIN1, CBS, CC2D2A, CCDC8, CCDC88C, CCN6, CD247, CD3D, CD3E, CD3G, CD40, CD40LG, CD8A, CDCA7, CDH23, CEP104, CEP290, CERKL, CERS3, CFTR, CHAT, CHMP1A, CHRNE, CHRNG, CHST6, CIB2, CIITA, CLCF1, CLCN1, CLCN5, CLN3, CLN5, CLN6, CLN8, CLP1, CLRN1, CNGA1, CNGB1, CNGB3, CNTNAP2, COASY, COL4A3, COL4A4, COL4A5, COL7A1, COLQ, CORO1A, CP, CPLANE1, CPS1, CPT1A, CPT2, CRLF1, CRTAP, CTC1, CTNS, CTSA, CTSD, CTSF, CTSK, CUL7, CWC27, CYBA, CYBB, CYP11A1, CYP11B1, CYP17A1, CYP1B1, CYP21A2, CYP27A1, CYP27B1, CYP4F22, CYP7B1, DBT, DCAF17, DCLRE1C, DDB2, DDC, DHCR7, DHDDS, DLD, DMD, DNMT3B, DOCK8, DOK7, DPYD, DTNBP1, DYNC2H1, DYSF, EDA, EFEMP2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, ELP1, EMD, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERCC8, ESCO2, ETFA, ETFB, ETFDH, ETHE1, EVC2, EXOSC3, EYS, F9, FA2H, FAH, FAM161A, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FBXL4, FHL1, FKBP10, FKRP, FKTN, FMO3, FMR1, FOXN1, FOXP3, FOXRED1, FRAS1, FREM2, FUCA1, G6PC1, GAA, GALC, GALE, GALK1, GALNS, GALT, GAMT, GATM, GBA1 (previously known as GBA), GBE1, GCDH, GFM1, GFPT1, GJB2, GLA, GLB1, GLDC, GLE1, GNE, GNPAT, GNPTAB, GNPTG, GNS, GPHN, GRHPR, GRIP1, GSS, GUSB, HADHA, HADHB, HAMP, HAX1, HBA1, HBA2, HBB, HCFC1, HELLS, HEXA, HEXB, HGSNAT, HINT1, HJV, HLCS, HMGCL, HOGA1, HPD, HPS1, HPS3, HPS4, HPS5, HPS6, HSD17B10, HSD17B4, HSD3B2, HYAL1, HYCC1 (previously known as FAM126A), HYLS1, IDS, IDUA, IFT140, IKBKB, IL2RA, IL2RG, IL7R, INPP5E, ITPA, IVD, JAK3, KCNJ1, KCTD7, KIF14, L1CAM, LAMA2, LAMA3, LAMB3, LAMC2, LAMP2, LARS1, LCA5, LCK, LHX3, LIFR, LIG4, LIPA, LIPN, LMBRD1, LOXHD1, LPL, LRAT, LRP2, LRPPRC, LTBP4, LYST, MAK, MALT1, MAN2B1, MANBA, MCCC1, MCCC2, MCEE, MCOLN1, MCPH1, MED17, MEFV, MESP2, MFSD8, MID1, MKKS, MKS1, MLC1, MMAA, MMAB, MMACHC, MMADHC, MMUT, MOCS1, MOCS2, MPI, MPL, MPV17, MTHFD1, MTM1, MTRR, MTTP, MVK, MYO7A, NAGA, NAGLU, NAGS, NBAS, NBN, NCF2, NCF4, NDUFAF2, NDUFAF5, NDUFS4, NDUFS6, NDUFS7, NDUFV1, NEB, NEU1, NGLY1, NHEJ1, NIPAL4, NONO, NPC1, NPC2, NPHP1, NPHP3, NPHS1, NPHS2, NR0B1, NTRK1, OAT, OBSL1, OCA2, OCRL, OPA3, OSTM1, OTC, OTOF, P3H1, PAH, PANK2, PC, PCBD1, PCCA, PCCB, PCDH15, PDHA1, PDHB, PDHX, PDP1, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PFKM, PGM3, PHGDH, PHKA1, PHKA2, PHKB, PHKG2, PKHD1, PLA2G6, PLEKHG5, PLOD2, PLP1, PMM2, PNP, PNPLA1, PNPO, POLG, POLH, POMGNT1, POMT1, POMT2, POR, POU3F4, PPIB, PPT1, PRCD, PRDM5, PRF1, PRKDC, PROP1, PSAP, PTPRC, PTS, PUS1, PYCR1, PYGM, QDPR, RAB23, RAG1, RAG2, RAPSN, RARS2, RD3, RDH12, RFX5, RFXANK, RFXAP, RLBP1, RMRP, RNASEH2A, RNASEH2B, RNASEH2C, RP2, RPE65, RPGR, RPGRIP1, RPGRIP1L, RPS6KA3, RS1, SACS, SAMHD1, SCO2, SDCCAG8, SDR9C7, SELENON, SEPSECS, SERPINF1, SGCA, SGCB, SGCD, SGCG, SGSH, SKIC2 (previously known as SKIV2L), SKIC3 (previously known as TTC37), SLC12A1, SLC12A6, SLC16A2, SLC17A5, SLC19A3, SLC22A5, SLC25A13, SLC25A15, SLC25A20, SLC26A2, SLC26A4, SLC27A4, SLC2A10, SLC35A3, SLC37A4, SLC39A4, SLC46A1, SLC4A11, SLC6A8, SLC7A7, SMARCAL1, SMN1, SMPD1, SP110, SPATA7, SPG11, SPG21, STAR, STK4, STX11, STXBP2, SUMF1, SUOX, SURF1, SYNE4, TAT, TAFAZZIN, TCIRG1, TCTN1, TCTN2, TCTN3, TECPR2, TF, TGM1, TH, TK2, TMEM138, TMEM216, TMEM231, TMEM237, TMEM38B, TMEM67, TMEM70, TNFSF11, TNXB, TPP1, TRAPPC11, TRIM32, TRMU, TSEN2, TSEN34, TSEN54, TSFM, TTC7A, TTC8, TTPA, TULP1, TYMP, TYR, UNC13D, UNG, USH1C, USH1G, USH2A, VLDLR, VPS13A, VPS13B, VPS45, VPS53, VRK1, WAS, WHRN, WNT1, WRN, XPA, XPC, ZAP70, ZBTB24 and ZNF469. |
Males are not tested for x-linked disorders, including fragile X syndrome.
Test orders must include an attestation that the provider has the patient's informed consent for genetic testing.
14 - 21 days (In some cases, additional time may be required for confirmatory or reflex tests.)
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
For more information, please view the literature below.
Clinical Questionnaire for Inheritest® Carrier Screen and GeneSeq® PLUS
Whole blood or Oragene Dx 500 saliva kit
Whole blood or Oragene Dx 500 saliva kit Whole blood or Oragene Dx 500 saliva kit |
Whole blood or Oragene Dx 500 saliva kit Whole blood or Oragene Dx 500 saliva kit |
8.5 mL whole blood or Oragene Dx saliva kit
8.5 mL whole blood or Oragene Dx saliva kit 8.5 mL whole blood or Oragene Dx saliva kit |
8.5 mL whole blood or Oragene Dx saliva kit 8.5 mL whole blood or Oragene Dx saliva kit |
3 mL whole blood or Oragene Dx saliva kit
Yellow-top (ACD-A) tube or lavender-top (EDTA) tube or Oragene Dx 500 saliva collection kit
Yellow-top (ACD-A) tube or lavender-top (EDTA) tube or Oragene Dx 500 saliva collection kit Yellow-top (ACD-A) tube or lavender-top (EDTA) tube or Oragene Dx 500 saliva collection kit |
Yellow-top (ACD-A) tube or lavender-top (EDTA) tube or Oragene Dx 500 saliva collection kit Yellow-top (ACD-A) tube or lavender-top (EDTA) tube or Oragene Dx 500 saliva collection kit |
Standard phlebotomy; follow Oragene Dx 500 saliva kit collection instructions. Do not eat, drink, smoke or chew gum 30 minutes prior to collection.
Standard phlebotomy; follow Oragene Dx 500 saliva kit collection instructions. Do not eat, drink, smoke or chew gum 30 minutes prior to collection. Standard phlebotomy; follow Oragene Dx 500 saliva kit collection instructions. Do not eat, drink, smoke or chew gum 30 minutes prior to collection. |
Standard phlebotomy; follow Oragene Dx 500 saliva kit collection instructions. Do not eat, drink, smoke or chew gum 30 minutes prior to collection. Standard phlebotomy; follow Oragene Dx 500 saliva kit collection instructions. Do not eat, drink, smoke or chew gum 30 minutes prior to collection. |
Maintain specimen at room temperature or refrigerate at 4°C. Do not freeze.
Whole blood: 4 days at room temperature or 4°C
Saliva: 60 days at room temperature
Whole blood: 4 days at room temperature or 4°C Saliva: 60 days at room temperature Whole blood: 4 days at room temperature or 4°C Saliva: 60 days at room temperature |
Whole blood: 4 days at room temperature or 4°C Saliva: 60 days at room temperature Whole blood: 4 days at room temperature or 4°C Saliva: 60 days at room temperature |
Frozen or hemolyzed specimen; quantity not sufficient for analysis; improper container or blood specimens more than four days post draw
This test is used for pan-ethnic carrier screening and includes more than 500 clinically relevant genetic disorders, including all the genes in the 14-Gene, 100 PLUS and 300 PLUS panels.
Technologies used do not detect germline mosaicism and do not rule out the presence of large chromosomal aberrations including rearrangements and gene fusions, or variants in regions or genes not included in this test, or possible inter/intragenic interactions between variants or repeat expansions.
Variant classification and/or interpretation may change over time if more information becomes available. False positive or false negative results may occur for reasons that include: rare genetic variants, sex chromosome abnormalities, pseudogene interference, blood transfusions, bone marrow transplantation, somatic or tissue-specific mosaicism, mislabeled samples or erroneous representation of family relationships.
This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration.
Next Generation Sequencing: Identifies genetic variants, including small nucleotide variants (SNVs), insertions, deletions and copy number variants (CNVs).
Spinal muscular atrophy (SMA): Copy number assessment of SMN1 exon 7 by quantitative polymerase chain reaction (qPCR). For carrier screening, when two copies of SMN1 are detected, allelic discrimination qPCR targeting c.*3+80T>G in SMN1 is performed. The presence or absence of c.*3+80T>G correlates with an increased or decreased risk, respectively, of being a silent carrier (2+0).
Fragile X syndrome: Polymerase chain reaction (PCR) followed by capillary electrophoresis, with reflex to AGG interruption analysis and methylation PCR analysis for positive samples.
Order Code | Order Code Name | Order Loinc | Result Code | Result Code Name | UofM | Result LOINC |
---|---|---|---|---|---|---|
481893 | Inheritest 500 PLUS Panel | 481875 | Genes | 48018-6 | ||
481893 | Inheritest 500 PLUS Panel | 481876 | Ethnicity | 46463-6 | ||
481893 | Inheritest 500 PLUS Panel | 481877 | Specimen Type | 31208-2 | ||
481893 | Inheritest 500 PLUS Panel | 481878 | Genetic Counselor | 89993-0 | ||
481893 | Inheritest 500 PLUS Panel | 481879 | Indication | 42349-1 | ||
481893 | Inheritest 500 PLUS Panel | 481880 | Result: | 19102-3 | ||
481893 | Inheritest 500 PLUS Panel | 481881 | Interpretation | 53039-4 | ||
481893 | Inheritest 500 PLUS Panel | 481882 | General Comments | 8262-8 | ||
481893 | Inheritest 500 PLUS Panel | 481883 | Recommendations | 62385-0 | ||
481893 | Inheritest 500 PLUS Panel | 481884 | Additional ClinicalInformation | 55752-0 | ||
481893 | Inheritest 500 PLUS Panel | 481885 | Comments | 8251-1 | ||
481893 | Inheritest 500 PLUS Panel | 481886 | Methods/Limitations | 49549-9 | ||
481893 | Inheritest 500 PLUS Panel | 481887 | References | 75608-0 | ||
481893 | Inheritest 500 PLUS Panel | 481888 | Disorders Tested | 19102-3 | ||
481893 | Inheritest 500 PLUS Panel | 481889 | Director Review/Release | 72486-4 | ||
481893 | Inheritest 500 PLUS Panel | 481890 | 51969-4 | |||
481893 | Inheritest 500 PLUS Panel | 481892 | Patient Gender | 76691-5 |
Reflex Table for Patient Gender | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 482148 | INH 500 PLUS + Fragile X | 482146 | INH 500 PLUS NGSBC | N/A |
Reflex Table for Patient Gender | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 482148 | INH 500 PLUS + Fragile X | 482147 | FRAXBC | N/A |
Reflex Table for Patient Gender | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 482149 | INH 500 PLUS NGSBC | 482149 | INH 500 PLUS NGSBC | N/A |
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