Medizinisches Versorgungszentrum DRK Blutspendedienst Frankfurt gemeinnützige
Official name: Medizinisches Versorgungszentrum DRK Blutspendedienst Frankfurt gemeinnützige GmbH
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Details
Frankfurt/Main 60528 , Germany
Accreditation
Transfusion medicine and clinical laboratory providing testing across clinical chemistry, immunology, human genetics, and transfusion medicine. Includes flow cytometric cell enumeration and particle counting on blood samples, alongside ligand assays via ELISA.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-13315-01-01
Status
ActiveSince
27 February 2026
Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.
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Test Capabilities (190)
| Standard Reference | Description | Category |
|---|---|---|
| AB0 System | AB0-System | Biocompatibility (ISO 10993) |
| Antikörper Screening | Antikörper-Screening | Biocompatibility (ISO 10993) |
| Antikörperscreening | HLA-Antikörper Screening | Biocompatibility (ISO 10993) |
| Arrhythmogene rechtsventrikuläre | Arrhythmogene rechtsventrikuläre | Biocompatibility (ISO 10993) |
| HLA Klasse II | HLA-Klasse II | Biocompatibility (ISO 10993) |
| (HBG1 und HBG2 ) | (HBG1 und HBG2 ) | Chromatography (GC, HPLC) |
| ACKR1 (Duffy-Blutgruppe) | ACKR1 (Duffy-Blutgruppe) | Chromatography (GC, HPLC) |
| Blutgruppe) | RHD, RHCE (Rh-Blutgruppe) | Chromatography (GC, HPLC) |
| Blutgruppen-Polymorphismen | Blutgruppen-Polymorphismen | Chromatography (GC, HPLC) |
| CD109 (HPA-15) | CD109 (HPA-15) | Chromatography (GC, HPLC) |
| FUT2 (Lewis-Blutgruppe) | FUT2 (Lewis-Blutgruppe) | Chromatography (GC, HPLC) |
| FUT3 (Lewis-Blutgruppe) | FUT3 (Lewis-Blutgruppe) | Chromatography (GC, HPLC) |
| GYPA, GYPB (MNS-Blutgruppe) | GYPA, GYPB (MNS-Blutgruppe) | Chromatography (GC, HPLC) |
| HJV , HAMP , TFR2 , SLC11A3 | HJV , HAMP , TFR2 , SLC11A3 | Chromatography (GC, HPLC) |
| Hereditäre Persistenz von | Hereditäre Persistenz von | Chromatography (GC, HPLC) |
| KEL (Kell-Blutgruppe) | KEL (Kell-Blutgruppe) | Chromatography (GC, HPLC) |
| SLC14A1 (Kidd-Blutgruppe) | SLC14A1 (Kidd-Blutgruppe) | Chromatography (GC, HPLC) |
| XK (Kx-Blutgruppe) | XK (Kx-Blutgruppe) | Chromatography (GC, HPLC) |
| morphismen (HPA-1, -2, 9 -15) (SSP-PCR) | morphismen (HPA-1, -2, 9 -15) (SSP-PCR) | Chromatography (GC, HPLC) |
| sonstige Hämoglobinopahtien | sonstige Hämoglobinopahtien | Chromatography (GC, HPLC) |
| (VWF:Ac) | (VWF:CB) | Clinical Chemistry |
| Blutgruppenallele | Blutgruppenallele | Elemental Analysis |
| Catecholaminerge polymorphe | Catecholaminerge polymorphe | Elemental Analysis |
| Hämatokrit | Hämatokrit | Elemental Analysis |
| MCV | MCV | Elemental Analysis |
| Erythrozytä re Antigene | Erythrozytäre Antigene | Food Safety Testing |
| Kell-Merkmal K | Kell-Merkmal K | Food Safety Testing |
| Rh-Untergruppen | Rh-Untergruppen | Food Safety Testing |
| - Basophile | Basophile | Hematology |
| - Eosinophile | Eosinophile | Hematology |
| - Erythrozyten | Erythrozyten | Hematology |
| - Leukozyten | Leukozyten | Hematology |
| - Lymphozyten | Lymphozyten | Hematology |
| - Monozyten | Monozyten | Hematology |
| - Thrombozyten | Thrombozyten | Hematology |
| Antikörpernachweis, Kreuzprobe mit DTT behandelten Erythrozyten | Antikörpernachweis, Kreuzprobe mit DTT-behandelten Erythrozyten | Hematology |
| Coombs-Test | Direkter Coombstest | Hematology |
| Direkter Antihumanglobulintest (DAT bzw. DCT) | Direkter Antihumanglobulintest (DAT bzw. DCT) | Hematology |
| Kreuzprobe | Kreuzprobe | Hematology |
| Neutrophile Granulozyten | Neutrophile Granulozyten | Hematology |
| Verträglichkeitsprobe | Verträglichkeitsprobe | Hematology |
| AB0 | Blutgruppe AB0 | Immunology / Serology |
| AB0-Blutgruppe und RhD | AB0-Blutgruppe und RhD | Immunology / Serology |
| Antigen D im indirekten | Antigen-D im indirekten | Immunology / Serology |
| Antikörper Differenzierung | Antikörperdifferenzierung | Immunology / Serology |
| Antikörper Differenzierung | Antikörper-Differenzierung | Immunology / Serology |
| Antikörper Titer | Hepatitis-B-Antikörper Titer | Immunology / Serology |
| Antikörper Titer | Antikörper-Titer | Immunology / Serology |
| Antikörperscreening | Antikörperscreening | Immunology / Serology |
| Coombstest | Coombstest | Immunology / Serology |
| Crossmatch (serologische Verträglichkeitsprobe im HLA- System) inklusive Auto-Crossmatch | Crossmatch (serologische Verträglichkeitsprobe im HLA- System) inklusive Auto-Crossmatch | Immunology / Serology |
| Gebundene Antikörper | Gebundene Antikörper | Immunology / Serology |
| HLA Klasse I (A/B/C) | HLA Klasse I (A/B/C) | Immunology / Serology |
| HLA-Antikörper Differenzierung | HLA-Antikörperdifferenzierung | Immunology / Serology |
| HLA-Antikörperscreening | HLA-Antikörperscreening | Immunology / Serology |
| Kreuzprobe/Serologische | Kreuzprobe/Serologische | Immunology / Serology |
| Lymphozyten CD34+ | Lymphozyten CD34+ | Immunology / Serology |
| Rh-Merkmal D | Rh-Merkmal D | Immunology / Serology |
| Rhesus-Formel und Kell-Antigen | Rhesusformel und Kell-Antigen | Immunology / Serology |
| Verträglichkeitsprobe im | Verträglichkeitsprobe im | Immunology / Serology |
| (ADAMTS13 ) | (ADAMTS13) | Molecular Diagnostics / PCR |
| (DSP, LMNA, SCN5A ) | (DSP, LMNA, SCN5A ) | Molecular Diagnostics / PCR |
| (F5-Gen: dbSNP rs6025) | Thrombophilie (F5-Gen: HR2 (dbSNP rs1800595)) | Molecular Diagnostics / PCR |
| (FGA, FGB, FGG) | Afibrinogenämie (FGA, FGB, FGG) | Molecular Diagnostics / PCR |
| (HBB) | Beta-Thalassämie (HBB) | Molecular Diagnostics / PCR |
| (ITGA2B, ITGB3) | (ITGA2B, ITGB3) | Molecular Diagnostics / PCR |
| (MYH7, CASQ2, MYBPC3, TNNT2 ) | (MYH7, CASQ2, MYBPC3, TNNT2 ) | Molecular Diagnostics / PCR |
| (SCN5A) | Brugada-Syndrom (SCN5A) | Molecular Diagnostics / PCR |
| (SSP-PCR) | (SSP-PCR) | Molecular Diagnostics / PCR |
| (TNNI3, MYH7, MYBPC3, FLNC ) | (TNNI3, MYH7, MYBPC3, FLNC ) | Molecular Diagnostics / PCR |
| A-, Dys-, Hypofibrinogenämie (FGA, FGB, FGG ) | A-, Dys-, Hypofibrinogenämie (FGA, FGB, FGG ) | Molecular Diagnostics / PCR |
| ABO-, Rh-, Kell-, Kidd-, Duffy-, MNSs- Blutgruppensystems (SSP-PCR) | ABO-, Rh-, Kell-, Kidd-, Duffy-, MNSs- Blutgruppensystems (SSP-PCR) | Molecular Diagnostics / PCR |
| ART4 (Exon 2) (Dombrock- Blutgruppe) | ART4 (Exon 2) (Dombrock- Blutgruppe) | Molecular Diagnostics / PCR |
| Alpha-Thalassämie (HBA1 , HBA2 ) | Alpha-Thalassämie (HBA1 , HBA2 ) | Molecular Diagnostics / PCR |
| Andersen-Tawil-Syndrom (KCNJ2 ) | Andersen-Tawil-Syndrom (KCNJ2 ) | Molecular Diagnostics / PCR |
| Angiödem (F12 ) | Angiödem (F12 ) | Molecular Diagnostics / PCR |
| Antithrombin-Mangel (SERPINC1 ) | Antithrombin-Mangel (SERPINC1 ) | Molecular Diagnostics / PCR |
| Arrhythmogene Kardiomyopathie | Arrhythmogene Kardiomyopathie | Molecular Diagnostics / PCR |
| Arrhythmogene Kardiomyopathie (DSP, LMNA, SCN5A, FLNC ) | Arrhythmogene Kardiomyopathie (DSP, LMNA, SCN5A, FLNC ) | Molecular Diagnostics / PCR |
| Arrhythmogene Kardiomyopathie (Illumina TruSight Cardio Panel, DSP, FLNC, LMNA, PLN, RBM20, DES, SCN5A, TMEM43 ) | Arrhythmogene Kardiomyopathie (Illumina TruSight Cardio Panel, DSP, FLNC, LMNA, PLN, RBM20, DES, SCN5A, TMEM43 ) | Molecular Diagnostics / PCR |
| Aspirin-Resistenz (COX1= PTGS1 ) | Aspirin-Resistenz (COX1= PTGS1 ) | Molecular Diagnostics / PCR |
| Autoimmunthrombozytopenie | Autoimmunthrombozytopenie | Molecular Diagnostics / PCR |
| Bernard-Soulier-Syndrom (GP1BA , GP1BB, GP9 , GP5 ) | Bernard-Soulier-Syndrom (GP1BA , GP1BB, GP9 , GP5 ) | Molecular Diagnostics / PCR |
| Beta-Thalassämie (HBB ) | Beta-Thalassämie (HBB ) | Molecular Diagnostics / PCR |
| Blutgruppen-Polymorphismen des | Blutgruppen-Polymorphismen des | Molecular Diagnostics / PCR |
| Brugada-Syndrom (Illumina TruSight Cardio Panel, SCN5A) | Brugada-Syndrom (Illumina TruSight Cardio Panel, SCN5A) | Molecular Diagnostics / PCR |
| Cardiac Conduction Disease (Illumina TruSight Cardio Panel, LMNA, SCN5A, TRPM4 ) | Cardiac Conduction Disease (Illumina TruSight Cardio Panel, LMNA, SCN5A, TRPM4 ) | Molecular Diagnostics / PCR |
| Cardiac Conduction Disease (LMNA, SCN5A) | Cardiac Conduction Disease (LMNA, SCN5A) | Molecular Diagnostics / PCR |
| Compaction-Kardiomyopathie | Non-compaction Kardiomyopathie | Molecular Diagnostics / PCR |
| Cumarin-Resistenz (VKORC1 und CYP2C9 ) | Cumarin-Resistenz (VKORC1 und CYP2C9 ) | Molecular Diagnostics / PCR |
| Cumarin-Sensitivität (CYP2C9 , VKORC1 und CYP4F2 ) | Cumarin-Sensitivität (CYP2C9 , VKORC1 und CYP4F2 ) | Molecular Diagnostics / PCR |
| Dilatative Kardiomyopathie | Dilatative Kardiomyopathie | Molecular Diagnostics / PCR |
| Dilatative Kardiomyopathie (LMNA, MYH7, MYBPC3, TNNT2, TNNI3, SCN5A, DSP, FLNC ) | Dilatative Kardiomyopathie (LMNA, MYH7, MYBPC3, TNNT2, TNNI3, SCN5A, DSP, FLNC ) | Molecular Diagnostics / PCR |
| Dissektionen (LOX, PRKG1) | Dissektionen (LOX, PRKG1) | Molecular Diagnostics / PCR |
| F13B) | Faktor XIII B-Mangel (F13B) | Molecular Diagnostics / PCR |
| Faktor-V-Mangel (F5 inklusive dbSNP r6027 ) | Faktor-V-Mangel (F5 inklusive dbSNP r6027 ) | Molecular Diagnostics / PCR |
| Faktor-XIII-Mangel (F13A1 und F13B); dbSNP rs5985 | Faktor-XIII-Mangel (F13A1 und F13B); dbSNP rs5985 | Molecular Diagnostics / PCR |
| HLA-A-Locus | HLA-A-Locus | Molecular Diagnostics / PCR |
| HLA-B-Locus | HLA-B-Locus | Molecular Diagnostics / PCR |
| HLA-C-Locus | HLA-C-Locus | Molecular Diagnostics / PCR |
| HLA-DPA1-Locus | HLA-DPA1-Locus | Molecular Diagnostics / PCR |
| HLA-DPB1 Locus | HLA-DPB1-Locus | Molecular Diagnostics / PCR |
| HLA-DQA1 | HLA-DQA1 | Molecular Diagnostics / PCR |
| HLA-DQA1-Locus | HLA-DQA1-Locus | Molecular Diagnostics / PCR |
| HLA-DQB1-Locus | HLA-DQB1-Locus | Molecular Diagnostics / PCR |
| HLA-DRB1 -Locus | HLA-DRB1-Locus | Molecular Diagnostics / PCR |
| HLA-DRB3/4/5-Locus | HLA-DRB3/4/5-Locus | Molecular Diagnostics / PCR |
| HLA-Klasse II (DRB1/DQA1/DQB1/DPA1/ DPB1/DRB3/DRB4/DRB5) | HLA-Klasse II (DRB1/DQA1/DQB1/DPA1/ DPB1/DRB3/DRB4/DRB5) | Molecular Diagnostics / PCR |
| Hereditäre Hämochromatose | Hereditäre Hämochromatose | Molecular Diagnostics / PCR |
| Hereditäre Hämochromatose (HFE , HJV , HAMP , TFR2 , SLC11A3 ) | Hereditäre Hämochromatose (HFE , HJV , HAMP , TFR2 , SLC11A3 ) | Molecular Diagnostics / PCR |
| Hereditäre Persistenz von HbF (HBG1 und HBG2 ) | Hereditäre Persistenz von HbF (HBG1 und HBG2 ) | Molecular Diagnostics / PCR |
| Hereditäre Thrombozytopenie (ADAMTS13 ) | Hereditäre Thrombozytopenie (ADAMTS13 ) | Molecular Diagnostics / PCR |
| Homocysteinurie (CBS und MTHFR ); MTHFR-Gen: dbSNP | Homocysteinurie (CBS und MTHFR ); MTHFR-Gen: dbSNP | Molecular Diagnostics / PCR |
| Hypertrophe Kardiomyopathie | Hypertrophe Kardiomyopathie | Molecular Diagnostics / PCR |
| Hypertrophe Kardiomyopathie (MYH7, MYBPC3, TNNT2, TNNI, FLNC, TTR ) | Hypertrophe Kardiomyopathie (MYH7, MYBPC3, TNNT2, TNNI, FLNC, TTR ) | Molecular Diagnostics / PCR |
| Hypo-, Dysthrombinämie (F2 ) | Hypo-, Dysthrombinämie (F2 ) | Molecular Diagnostics / PCR |
| Hämophilie B (F9 ) | Hämophilie B (F9 ) | Molecular Diagnostics / PCR |
| ITGA2 (HPA-5), ITGB3 (HPA-1/-4/- 6), ITGA2B (HPA-3/-9), GP1BA (HPA- 2) | ITGA2 (HPA-5), ITGB3 (HPA-1/-4/- 6), ITGA2B (HPA-3/-9), GP1BA (HPA- 2) | Molecular Diagnostics / PCR |
| Infantile und neonatale | Infantile und neonatale | Molecular Diagnostics / PCR |
| Kardiomyopathie (Illumina TruSight Cardio Panel, PKP2, DSC2, DSP, DSG2, JUP, DES, TMEM43, PLN) | Kardiomyopathie (Illumina TruSight Cardio Panel, PKP2, DSC2, DSP, DSG2, JUP, DES, TMEM43, PLN) | Molecular Diagnostics / PCR |
| Kardiomyopathie (PKP2, DSC2, DSP, DSG2 ); MLPA: PKP2, DSG2, DSC2, JUP, DSP, TGFß3, RYR2 | Kardiomyopathie (PKP2, DSC2, DSP, DSG2 ); MLPA: PKP2, DSG2, DSC2, JUP, DSP, TGFß3, RYR2 | Molecular Diagnostics / PCR |
| Kardiomyopathie (PKP2, DSG2, SCN5A ) | Kardiomyopathie (PKP2, DSG2, SCN5A ) | Molecular Diagnostics / PCR |
| Kininogen-Mangel, High molecular | Kininogen-Mangel, High molecular | Molecular Diagnostics / PCR |
| Kombinierter Faktor-II, -VII, -IX, -X- Mangel (GGCX und VKORC1 ) | Kombinierter Faktor-II, -VII, -IX, -X- Mangel (GGCX und VKORC1 ) | Molecular Diagnostics / PCR |
| Kombinierter Faktor-V und Faktor | Kombinierter Faktor-V und Faktor | Molecular Diagnostics / PCR |
| Loeys-Dietz-Syndrom (Illumina TruSight Cardio Panel, SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 ) | Loeys-Dietz-Syndrom (Illumina TruSight Cardio Panel, SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 ) | Molecular Diagnostics / PCR |
| Long-QT-Syndrom (CLCN1, KCNH2, KCNE1, KCNE2, KCNJ2, KCNQ1 ) | Long-QT-Syndrom (CLCN1, KCNH2, KCNE1, KCNE2, KCNJ2, KCNQ1 ) | Molecular Diagnostics / PCR |
| Long-QT-Syndrom (Illumina TruSight Cardio Panel, KCNQ1, KCNH2, KCNJ2, SCN5A, KCNE1, CACNA1C, CALM1, CALM2, CALM3, TRDN ) | Long-QT-Syndrom (Illumina TruSight Cardio Panel, KCNQ1, KCNH2, KCNJ2, SCN5A, KCNE1, CACNA1C, CALM1, CALM2, CALM3, TRDN ) | Molecular Diagnostics / PCR |
| Long-QT-Syndrom (KCNQ1, KCNH2, SCN5A, KCNE1, KCNJ2, CACNA1C, CALM2, CALM3) | Long-QT-Syndrom (KCNQ1, KCNH2, SCN5A, KCNE1, KCNJ2, CACNA1C, CALM2, CALM3) | Molecular Diagnostics / PCR |
| MYLK, TGFBR1, TGFBR2 | MYLK, TGFBR1, TGFBR2 | Molecular Diagnostics / PCR |
| Mangel/Dysplasminogenämie | Mangel/Dysplasminogenämie | Molecular Diagnostics / PCR |
| Marfan-Syndrom (Illumina TruSight Cardio Panel, FBN1, TGFBR1, TGFBR2 ) | Marfan-Syndrom (Illumina TruSight Cardio Panel, FBN1, TGFBR1, TGFBR2 ) | Molecular Diagnostics / PCR |
| Morbus Fabry (Illumina TruSight Cardio Panel, GLA ) | Morbus Fabry (Illumina TruSight Cardio Panel, GLA ) | Molecular Diagnostics / PCR |
| Morbus Glanzmann (ITGA2B und ITGB3 ) | Morbus Glanzmann (ITGA2B und ITGB3 ) | Molecular Diagnostics / PCR |
| Neonatale | Neonatale | Molecular Diagnostics / PCR |
| Non-Compaction Kardiomyopathie (MYH7, CASQ2, MYBPC3, TNNI3, TNNT2, DSP, LMNA ) | Non-Compaction Kardiomyopathie (MYH7, CASQ2, MYBPC3, TNNI3, TNNT2, DSP, LMNA ) | Molecular Diagnostics / PCR |
| PAI1-Mangel (PAI1= SERPINE1 ); dbSNP rs1799889 | PAI1-Mangel (PAI1= SERPINE1 ); dbSNP rs1799889 | Molecular Diagnostics / PCR |
| Plasminogen-Mangel/ Dysplasminogenämie (PLG ) | Plasminogen-Mangel/ Dysplasminogenämie (PLG ) | Molecular Diagnostics / PCR |
| Protein-C-Mangel (PROC ) | Protein-C-Mangel (PROC ) | Molecular Diagnostics / PCR |
| Protein-C-Rezeptor-Mangel (PROC ) | Protein-C-Rezeptor-Mangel (PROC ) | Molecular Diagnostics / PCR |
| Protein-S-Mangel (PROS1 ) | Protein-S-Mangel (PROS1 ) | Molecular Diagnostics / PCR |
| Protein-Z-Mangel (PROZ ) | Protein-Z-Mangel (PROZ ) | Molecular Diagnostics / PCR |
| Präkallikrein-Mangel (KLKB1 ) | Präkallikrein-Mangel (KLKB1 ) | Molecular Diagnostics / PCR |
| Quebec platelet disorder (MMRN1 und PLAU) | Quebec platelet disorder (MMRN1 und PLAU) | Molecular Diagnostics / PCR |
| RHAG | RHAG | Molecular Diagnostics / PCR |
| RHCE | RHCE | Molecular Diagnostics / PCR |
| RHD | RHD | Molecular Diagnostics / PCR |
| RYR2, CASQ2, KCNJ2, TRDN | RYR2, CASQ2, KCNJ2, TRDN | Molecular Diagnostics / PCR |
| Restriktive Kardiomyopathie | Restriktive Kardiomyopathie | Molecular Diagnostics / PCR |
| Restriktive Kardiomyopathie (Illumina TruSight Cardio Panel, TNNI3, DES, MYH7, MYBPC3, TNNT2, ACTC1, FHL1, FLNC, GLA, MYL2, TPM1, TTR ) | Restriktive Kardiomyopathie (Illumina TruSight Cardio Panel, TNNI3, DES, MYH7, MYBPC3, TNNT2, ACTC1, FHL1, FLNC, GLA, MYL2, TPM1, TTR ) | Molecular Diagnostics / PCR |
| Restriktive Kardiomyopathie (TNNI3, MYH7, MYBPC3, TNNT2, FLNC ) | Restriktive Kardiomyopathie (TNNI3, MYH7, MYBPC3, TNNT2, FLNC ) | Molecular Diagnostics / PCR |
| Short-QT-Syndrom (Illumina TruSight Cardio Panel, KCNH2, KCNJ2, KCNQ1 | Short-QT-Syndrom (Illumina TruSight Cardio Panel, KCNH2, KCNJ2, KCNQ1) | Molecular Diagnostics / PCR |
| Short-QT-Syndrom (KCNH2, KCNJ2, KCNQ1) | Short-QT-Syndrom (KCNH2, KCNJ2, KCNQ1) | Molecular Diagnostics / PCR |
| Sichelzellkrankheit (HBS ) | Sichelzellkrankheit (HBS ) | Molecular Diagnostics / PCR |
| TCAP, TNNC1, TPM1, GLA | TCAP, TNNC1, TPM1, GLA | Molecular Diagnostics / PCR |
| Thorakale Aortenaneurysmen | Thorakale Aortenaneurysmen | Molecular Diagnostics / PCR |
| Thorakale Aortenaneurysmen und Dissektionen (Illumina TruSight Cardio Panel, ACTA2, LOX, MYH11, MYLK, PRKG1, TGFBR1, TGFBR2 ) | Thorakale Aortenaneurysmen und Dissektionen (Illumina TruSight Cardio Panel, ACTA2, LOX, MYH11, MYLK, PRKG1, TGFBR1, TGFBR2 ) | Molecular Diagnostics / PCR |
| Thorakale Aortenaneurysmen und Dissektionen (LOX, PRKG1) | Thorakale Aortenaneurysmen und Dissektionen (LOX, PRKG1) | Molecular Diagnostics / PCR |
| Thrombozytenblutgruppen-Poly- morphismen (HPA-1, -2, -3, -4, -5,-6,- 9 -15) (SSP-PCR) | Thrombozytenblutgruppen-Poly- morphismen (HPA-1, -2, -3, -4, -5,-6,- 9 -15) (SSP-PCR) | Molecular Diagnostics / PCR |
| VIII-Mangel (LMAN1 und MCFD2 ) | VIII-Mangel (LMAN1 und MCFD2 ) | Molecular Diagnostics / PCR |
| Ventrikuläre Tachykardie | ventrikuläre Tachykardie | Molecular Diagnostics / PCR |
| rs1801133, dbSNP rs1801131 | rs1801133, dbSNP rs1801131 | Molecular Diagnostics / PCR |
| sonstige Hämoglobinopathien (HbE , HbC , HbD ) | sonstige Hämoglobinopathien (HbE , HbC , HbD ) | Molecular Diagnostics / PCR |
| ventrikuläre Tachykardie (Illumina TruSight Cardio Panel, CALM1, CALM2, CALM3, RYR2, CASQ2, KCNJ2, TRDN, TECRL ) | ventrikuläre Tachykardie (Illumina TruSight Cardio Panel, CALM1, CALM2, CALM3, RYR2, CASQ2, KCNJ2, TRDN, TECRL ) | Molecular Diagnostics / PCR |
| ventrikuläre Tachykardie (RYR2, CASQ2, KCNJ2, CALM2, CALM3, TECRL ) | ventrikuläre Tachykardie (RYR2, CASQ2, KCNJ2, CALM2, CALM3, TECRL ) | Molecular Diagnostics / PCR |
| weight kininogen deficiency | weight kininogen deficiency | Molecular Diagnostics / PCR |
| weight kininogen deficiency (KNG ) | weight kininogen deficiency (KNG ) | Molecular Diagnostics / PCR |
| weitere Blutgruppensysteme (Kell, Duffy, Kidd, MNS) und seltene | weitere Blutgruppensysteme (Kell, Duffy, Kidd, MNS) und seltene | Molecular Diagnostics / PCR |
| (Illumina TruSight Cardio | (Illumina TruSight Cardio | Other |
| Kardiomyopathie (Illumina | Kardiomyopathie (Illumina | Other |
| (CO2) | (CO2) | Spectroscopy (XRF, ICP, AAS) |
| A-, Dys-, Hypofibrinogenämie | A-, Dys-, Hypofibrinogenämie | Spectroscopy (XRF, ICP, AAS) |
| Bernard-Soulier-Syndrom | Bernard-Soulier-Syndrom | Spectroscopy (XRF, ICP, AAS) |
| Fa ktor-VII-Mangel (F7 ) | Faktor-VII-Mangel (F7 ) | Spectroscopy (XRF, ICP, AAS) |
| Faktor-X-Mangel (F10 ) | Faktor-X-Mangel (F10 ) | Spectroscopy (XRF, ICP, AAS) |
| Faktor-XI-Mangel (F11 ) | Faktor-XI-Mangel (F11 ) | Spectroscopy (XRF, ICP, AAS) |
| Faktor-XII-Mangel und hereditäres | Faktor-XII-Mangel und hereditäres | Spectroscopy (XRF, ICP, AAS) |
| HLA-Klasse II (DR/DQ/DP) | HLA-Klasse II (DR/DQ/DP) | Spectroscopy (XRF, ICP, AAS) |
| Hereditäre Thrombozytopenie | Hereditäre Thrombozytopenie | Spectroscopy (XRF, ICP, AAS) |
| Hypo-, Dysthrombinämie | Hypo-, Dysthrombinämie | Spectroscopy (XRF, ICP, AAS) |
| Hämoglobin | Hämoglobin | Spectroscopy (XRF, ICP, AAS) |
| Hämophilie A (F8 ) | Hämophilie A (F8 ) | Spectroscopy (XRF, ICP, AAS) |
| Hämophilie B (F9 ) | Hämophilie B(F9 ) | Spectroscopy (XRF, ICP, AAS) |
| Kininogen-Mangel, High | Kininogen-Mangel, High | Spectroscopy (XRF, ICP, AAS) |
| PAI1-Mangel (PAI1 ) | PAI1-Mangel (PAI1 ) | Spectroscopy (XRF, ICP, AAS) |
| Plasminogen | Plasminogen | Spectroscopy (XRF, ICP, AAS) |
| Protein-C-Rezeptor-Mangel | Protein-C-Rezeptor-Mangel | Spectroscopy (XRF, ICP, AAS) |
| Quebec platelet disorder | Quebec platelet disorder | Spectroscopy (XRF, ICP, AAS) |
| TAFI-Mangel (CPB2 ) | TAFI-Mangel (CPB2 ) | Spectroscopy (XRF, ICP, AAS) |
| VWF-Multimere | vWF-Multimere | Temperature / Pressure |
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