ScopeGenetik Berlin-Lichtenberg GmbH ÖBAG Medicover Humangenetik Berlin - Medicover Humangenetik Berlin-Lichtenberg MVZ Nebenbetriebsstätte Labor
26 capabilities
Accredited since December 2025
Verified May 2026
One of 3,188 in Germany
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Details
Plauener Straße 163-165
Berlin 13053 , Germany
Berlin 13053 , Germany
Accreditation
Active
DAkkS
D-ML-22602-01-01
Conducts molecular human genetics testing including PCR-based fragment length analysis and DNA sequencing to detect genetic abnormalities such as azoospermia-related microdeletions from blood and DNA samples.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-22602-01-01
Status
ActiveSince
08 December 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 (26)
| Standard Reference | Description | Category |
|---|---|---|
| Angeborener Chromosomensatz | angeborener Chromosomensatz | Biocompatibility (ISO 10993) |
| Erworbener Chromosomensatz | erworbener Chromosomensatz | Biocompatibility (ISO 10993) |
| Chorea Huntington (HTT) | Chorea Huntington (HTT) | Elemental Analysis |
| Cystische Fibrose (CFTR) | Cystische Fibrose (CFTR) | Elemental Analysis |
| (ATXN1); Typ 2 (ATXN2); Typ 3 | (ATXN1); Typ 2 (ATXN2); Typ 3 | Molecular Diagnostics / PCR |
| (ATXN3); Typ 6 (CACNA1A); Typ | (ATXN3); Typ 6 (CACNA1A); Typ | Molecular Diagnostics / PCR |
| (ATXN7); Typ 17(TBP) | (ATXN7); Typ 17(TBP) | Molecular Diagnostics / PCR |
| (CYP11B1, CYP17A1, HSD3B2, POR, STAR) | (CYP11B1, CYP17A1, HSD3B2, POR, STAR) | Molecular Diagnostics / PCR |
| (SHOX ) | Kleinwuchs (SHOX) | Molecular Diagnostics / PCR |
| (SNM1/SNM2) | (SNM1/SNM2) | Molecular Diagnostics / PCR |
| AZO-Panel (ADGRG2, AR, DMRT1, NR5A1, STAG3, TEX11, TEX14, TEX15) | AZO-Panel (ADGRG2, AR, DMRT1, NR5A1, STAG3, TEX11, TEX14, TEX15) | Molecular Diagnostics / PCR |
| Adrenogenitales Syndrom | Adrenogenitales Syndrom | Molecular Diagnostics / PCR |
| Alpha und BetaThalassämie (HBA1, HBA2,HBB) | Alpha und BetaThalassämie (HBA1, HBA2,HBB) | Molecular Diagnostics / PCR |
| Angelman Syndrom | Prader Willi Angelman Syndrom | Molecular Diagnostics / PCR |
| Azoospermie (AZF-Mikrodeletionen) | Azoospermie (AZF-Mikrodeletionen) | Molecular Diagnostics / PCR |
| Becker (DMD-Gen) | Becker (DMD-Gen) | Molecular Diagnostics / PCR |
| Beckwith-Wiedeman Syndrom | Beckwith-Wiedeman Syndrom | Molecular Diagnostics / PCR |
| Fragiles X-Syndrom (FMR1) | Fragiles X-Syndrom (FMR1) | Molecular Diagnostics / PCR |
| Hereditäre Fiebersyndrome (MEFV, MVK, NLRP3, TNFRSF1A) | Hereditäre Fiebersyndrome (MEFV, MVK, NLRP3, TNFRSF1A) | Molecular Diagnostics / PCR |
| Medicover Carrier-Screening Panel: | Medicover Carrier-Screening Panel: | Molecular Diagnostics / PCR |
| Muskeldystrophie Duchenne / | Muskeldystrophie Duchenne / | Molecular Diagnostics / PCR |
| Panel (BMP15, DIAPH2, ESR1, FIGLA, FMR1, FOXL2, FSHR, GDF9, INHA, LHCGR, NOBOX, NR5A1, POF1B, SOHLH1, SOHLH2, STAG3) | Panel (BMP15, DIAPH2, ESR1, FIGLA, FMR1, FOXL2, FSHR, GDF9, INHA, LHCGR, NOBOX, NR5A1, POF1B, SOHLH1, SOHLH2, STAG3) | Molecular Diagnostics / PCR |
| SMN1; Spinale Muskelatrophie | SMN1; Spinale Muskelatrophie | Molecular Diagnostics / PCR |
| Silver-Russel Syndrom | Silver-Russel-Syndrom | Molecular Diagnostics / PCR |
| Spinocerebelläre Ataxie Typ1 | Spinocerebelläre Ataxie Typ1 | Molecular Diagnostics / PCR |
| (ABCA3, ABCC8, ABCD1, ACADM, ACADVL, ACAT1, AFF2, AGA, AGXT, AHI1, AIRE, ALDOB, ALPL, ANO10, ARSA, ARX, ASL, ASPA, ATP7B, BBS1, BBS2, BCKDHB, BLM, BTD, CBS, CC2D2A, CCDC88C, CEP290, CFTR, CHRNE, CLCN1, CLRN1, CNGB3, COL7A1, CPT2, CYP11A1, CYP27A1, CYP27B1, DHCR7, DHDDS, DLD, DMD, DYNC2H1, ELP1, ERCC2, EVC2, F8, F9, FAH, FANCC, FKRP, FKTN, FMO3, FMR1, FXN, G6PC, GAA, GALT, GBA, GBE1, GJB2, GLA, GNPTAB, GRIP1, HEXA, HPS1, HPS3, IDUA, L1CAM, LRP2, MCCC2, MCOLN1, MCPH1, MID1, MLC1, MMACHC, MMUT, MVK, NAGA, NEB, NPHS1, NR0B1, OCA2, OTC, PAH, PCDH15, PKHD1, PLP1, PMM2, POLG, PRF1, RARS2, RNASEH2B, RPGR, RS1, SCO2, SLC19A3, SLC26A2, SLC26A4, SLC37A4, SLC6A8, SMN1, SMPD1, TF, | (ABCA3, ABCC8, ABCD1, ACADM, ACADVL, ACAT1, AFF2, AGA, AGXT, AHI1, AIRE, ALDOB, ALPL, ANO10, ARSA, ARX, ASL, ASPA, ATP7B, BBS1, BBS2, BCKDHB, BLM, BTD, CBS, CC2D2A, CCDC88C, CEP290, CFTR, CHRNE, CLCN1, CLRN1, CNGB3, COL7A1, CPT2, CYP11A1, CYP27A1, CYP27B1, DHCR7, DHDDS, DLD, DMD, DYNC2H1, ELP1, ERCC2, EVC2, F8, F9, FAH, FANCC, FKRP, FKTN, FMO3, FMR1, FXN, G6PC, GAA, GALT, GBA, GBE1, GJB2, GLA, GNPTAB, GRIP1, HEXA, HPS1, HPS3, IDUA, L1CAM, LRP2, MCCC2, MCOLN1, MCPH1, MID1, MLC1, MMACHC, MMUT, MVK, NAGA, NEB, NPHS1, NR0B1, OCA2, OTC, PAH, PCDH15, PKHD1, PLP1, PMM2, POLG, PRF1, RARS2, RNASEH2B, RPGR, RS1, SCO2, SLC19A3, SLC26A2, SLC26A4, SLC37A4, SLC6A8, SMN1, SMPD1, TF, | Other |
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