Genetik Berlin-Lichtenberg GmbH ÖBAG Medicover Humangenetik Berlin - Medicover Humangenetik Berlin-Lichtenberg MVZ Nebenbetriebsstätte Labor | ISO 17025 Lab in Berlin

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

Active

Since

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 PDF

Send an Enquiry

Request a quote, ask about capacity, or discuss your testing requirements directly with this lab.

Your name *

Your email *

Company *

Test method / standard Please select a test method from the list

Material / sample type

Number of samples / specimens

Timeline

Volume

Additional details (optional)

Genetik Berlin-Lichtenberg GmbH ÖBAG Medicover Humangenetik Berlin - Medicover Humangenetik Berlin-Lichtenberg MVZ Nebenbetriebsstätte Labor

DAkkS № D-ML-22602-01-01

Direct & private Your message goes straight to the lab

No obligation Free to enquire, no commitment required

What happens next?

We send your enquiry to the lab
The lab will review your enquiry and reply directly to your email
You agree on testing scope, timeline, and pricing

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
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
Prader Willi Angelman Syndrom	Prader Willi Angelman Syndrom	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