ScopeMVZ genetikum
Official name: MVZ genetikum GmbH
67 capabilities
Accredited since November 2025
Verified Oct 2026
One of 3,209 in Germany
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Details
Wegenerstraße 15
Neu-Ulm 89231 , Germany
Neu-Ulm 89231 , Germany
Accreditation
Active
DAkkS
D-ML-22061-01-01
genetikum.de
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Specializes in molecular human genetics and cytogenetics with capability to modify and develop genetic testing procedures, including PCR-based fragment length analysis and Sanger sequencing of blood and DNA samples.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-22061-01-01
Status
ActiveSince
10 November 2025
Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.
Download Scope PDFAdditional scope documents
Test Capabilities (67)
| Standard Reference | Description | Category |
|---|---|---|
| Angeborener Chromosomensatz | angeborener Chromosomensatz | Biocompatibility (ISO 10993) |
| AZFa-c | AZFa-c | Biological / Microbiological |
| Druckläsion (HNPP) | Druckläsion (HNPP) | Biological / Microbiological |
| Duchennesche/Beckersche | Duchennesche/Beckersche | Biological / Microbiological |
| Dysplasie (ACH, HCH, TD) | Dysplasie (ACH, HCH, TD) | Biological / Microbiological |
| Glykogenose Typ II (Pompe) | Glykogenose Typ II (Pompe) | Biological / Microbiological |
| Hämochromatose (H63D, C282Y) | Hämochromatose (H63D, C282Y) | Biological / Microbiological |
| Muskeldystrophie (DMD, BMD) | Muskeldystrophie (DMD, BMD) | Biological / Microbiological |
| Myotone Dystrophie (DM1) | Myotone Dystrophie (DM1) | Biological / Microbiological |
| Schwerhörigkeit (Cx26 ) | Schwerhörigkeit (Cx26 ) | Biological / Microbiological |
| fra(X)-Syndrom | fra(X)-Syndrom | Biological / Microbiological |
| (kundenspezifisches Gen-Panel) | (kundenspezifisches Gen-Panel) | Elemental Analysis |
| Alpha 1-Antitrypsin-Mangel | Alpha-1-Antitrypsin-Mangel | Elemental Analysis |
| Epilepsie-Panel SLC2A1 | Epilepsie-Panel SLC2A1 | Elemental Analysis |
| Genetikum-Panel | Genetikum-Panel | Elemental Analysis |
| Markerchromosomen-Abklärung | Markerchromosomen-Abklärung | Elemental Analysis |
| Mikroduplikationssyndrome | Mikroduplikationssyndrome | Elemental Analysis |
| PTPN11 | PTPN11 | Elemental Analysis |
| Subtelomeranalyse | Subtelomeranalyse | Elemental Analysis |
| Whole Exome Sequenzierung (WES) | Whole Exome Sequenzierung (WES) | Elemental Analysis |
| (GLUT1) | (GLUT1) | Molecular Diagnostics / PCR |
| Achondroplasie, Hypochondroplasie, Thanatophore | Achondroplasie, Hypochondroplasie, Thanatophore | Molecular Diagnostics / PCR |
| Adrenogenitales Syndrom (AGS) | Adrenogenitales-Syndrom (AGS) | Molecular Diagnostics / PCR |
| Angelman Syndrom | Angelman-Syndrom | Molecular Diagnostics / PCR |
| BRCA1 | BRCA1 | Molecular Diagnostics / PCR |
| BRCA1/BRCA2 | BRCA1/BRCA2: ID001 | Molecular Diagnostics / PCR |
| Brust- und Eierstockkrebs | Brust- und Eierstockkrebs: ATM, BRCA1*, BRCA2*, BRIP1, CHEK2, CDH1, PALB2, RAD51C, RAD51D, TP53*, NBN | Molecular Diagnostics / PCR |
| CFTR | CFTR | Molecular Diagnostics / PCR |
| CYP21A2 | CYP21A2 | Molecular Diagnostics / PCR |
| Chorea Huntington | Chorea-Huntington | Molecular Diagnostics / PCR |
| Cystische Fibrose | Cystische Fibrose: Screening der | Molecular Diagnostics / PCR |
| DHCR7 | DHCR7 | Molecular Diagnostics / PCR |
| DMD | DMD | Molecular Diagnostics / PCR |
| DMPK | DMPK | Molecular Diagnostics / PCR |
| FGFR3 | OMIM*176943, FGFR3 | Molecular Diagnostics / PCR |
| FMR1 | FMR1 | Molecular Diagnostics / PCR |
| GAA | GAA | Molecular Diagnostics / PCR |
| GJB2 | GJB2 | Molecular Diagnostics / PCR |
| GLA | GLA | Molecular Diagnostics / PCR |
| Glukose-Transporter-Defizienz | Glukose-Transporter-Defizienz | Molecular Diagnostics / PCR |
| HFE | HFE | Molecular Diagnostics / PCR |
| HTT | HTT | Molecular Diagnostics / PCR |
| MECP2 | MECP2 | Molecular Diagnostics / PCR |
| Markeranalyse | STR-Markeranalyse | Molecular Diagnostics / PCR |
| Morbus Fabry | Morbus Fabry: GLA | Molecular Diagnostics / PCR |
| Morbus Meulengracht (Gilbert- Syndrom), Crigler-Najjar-Syndrom | Morbus Meulengracht (Gilbert- Syndrom), Crigler-Najjar-Syndrom | Molecular Diagnostics / PCR |
| Morbus Meulengracht UGT1A1 | Morbus Meulengracht UGT1A1 | Molecular Diagnostics / PCR |
| Noonan-Syndrom (NS1), LEOPARD- Syndrom (LPRD1) | Noonan-Syndrom (NS1), LEOPARD- Syndrom (LPRD1) | Molecular Diagnostics / PCR |
| PMP22 | PMP22 | Molecular Diagnostics / PCR |
| Prader Willi Syndrom | Prader-Willi-Syndrom: Methylierungsstatus und Deletions/Duplikationsanalyse | Molecular Diagnostics / PCR |
| Rett Syndrom | Rett-Syndrom: MECP2 | Molecular Diagnostics / PCR |
| SERPINA1 | SERPINA1 | Molecular Diagnostics / PCR |
| SHOX | SHOX | Molecular Diagnostics / PCR |
| SHOX-Defizienz | SHOX-Defizienz: Leri-Weill-Dyschondrosteose | Molecular Diagnostics / PCR |
| Smith-Lemli-Opitz-Syndrom (SLOS) | Smith-Lemli-Opitz-Syndrom (SLOS) | Molecular Diagnostics / PCR |
| UBE3A | UBE3A | Molecular Diagnostics / PCR |
| spinobulbäre Muskelatrophie (Typ Kennedy) | spinobulbäre Muskelatrophie (Typ Kennedy) | Molecular Diagnostics / PCR |
| ABRAXAS1, ACD, ACTA2, ACTC1, | ABRAXAS1, ACD, ACTA2, ACTC1, | Other |
| ADGRG2, AIP, AKT1, AKT2, AKT3, | ADGRG2, AIP, AKT1, AKT2, AKT3, | Other |
| AR | AR | Other |
| Charcot-Marie-Tooth-Krankheit, demyelinisierend, Typ 1A (CMT1A), Hereditäre Neuropathie mit | Charcot-Marie-Tooth-Krankheit, demyelinisierend, Typ 1A (CMT1A), Hereditäre Neuropathie mit | Other |
| Fortsetzung: MSH3, MSH4, MSH6, | Fortsetzung: MSH3, MSH4, MSH6, | Other |
| Mikrodeletions- und | Mikrodeletions- und | Other |
| Pränataler PCR Schnelltest: | Pränataler PCR Schnelltest: | Other |
| Spinale Muskelatrophie (SMA) | Spinale Muskelatrophie (SMA): | Other |
| Azoospermiefaktor | Azoospermiefaktor | Sterility Testing |
| SMN1 | SMN1 | Sterility Testing |
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