MVZ genetikum

Official name: MVZ genetikum GmbH

69 capabilities Accredited since November 2025 Verified Apr 2026 One of 3,039 in Germany

Details

WegenerstraĂźe 15
Neu-Ulm 89231 , Germany

Accreditation

Active DAkkS D-ML-22061-01-01
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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

Active

Since

10 November 2025

Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.

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69 capabilities

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Test Capabilities (69)

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
Hypochondroplasie, Thanatophore Hypochondroplasie, Thanatophore 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
Pränataler PCR Schnelltest: Pränataler PCR Schnelltest: Chromatography (GC, HPLC)
(kundenspezifisches Gen-Panel) (kundenspezifisches Gen-Panel) Elemental Analysis
31 Mutationen im CFTR 31 Mutationen im CFTR Elemental Analysis
ALK, APC, APOB, AR, ARID1A, ARID1B, ARID2, ATM, ATP7B, ATR, AXIN2, BAP1, BARD1, BLM, BMP15, BMPR1A, BRCA1, BRCA2, BRIP1, BTG4, C11orf80, CACNA1S, CASR, CCND2, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, CDKN2B, CEBPA, CFTR, CHEK2, COL3A1, CPA1, CTRC, CYP11B1, CYP17A1, CYP19A1, DDB2, DIAPH2, DICER1, DIS3L2, DMRT1, DPF2, DSC2, DSG2, DSP, EGFR, EPCAM, EPHB4, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERCC8, EXT1, EXT2, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FBN1, FGFR1, FH, FIGLA, FLCN, FOXL2, FSHR, GALNT12, GATA2, GLA, GNA11, GNAQ, GNAS, GPC3, GREM1, HDAC8, HFE, HFM1, HOXB13, HRAS, HSD3B2, KCNH2, KCNJ2, KCNQ1, KDM6A, KHDC3L, KIF1B, KIT, KLHL10, KMT2D, KRAS, LDLR, LMNA, LZTR1, M1AP, MAX, MC1R, MCM9, MEI1, MEN1, MET, MITF, MLH1, MLH3, MRE11, MSH2, ALK, APC, APOB, AR, ARID1A, ARID1B, ARID2, ATM, ATP7B, ATR, AXIN2, BAP1, BARD1, BLM, BMP15, BMPR1A, BRCA1, BRCA2, BRIP1, BTG4, C11orf80, CACNA1S, CASR, CCND2, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, CDKN2B, CEBPA, CFTR, CHEK2, COL3A1, CPA1, CTRC, CYP11B1, CYP17A1, CYP19A1, DDB2, DIAPH2, DICER1, DIS3L2, DMRT1, DPF2, DSC2, DSG2, DSP, EGFR, EPCAM, EPHB4, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERCC8, EXT1, EXT2, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FBN1, FGFR1, FH, FIGLA, FLCN, FOXL2, FSHR, GALNT12, GATA2, GLA, GNA11, GNAQ, GNAS, GPC3, GREM1, HDAC8, HFE, HFM1, HOXB13, HRAS, HSD3B2, KCNH2, KCNJ2, KCNQ1, KDM6A, KHDC3L, KIF1B, KIT, KLHL10, KMT2D, KRAS, LDLR, LMNA, LZTR1, M1AP, MAX, MC1R, MCM9, MEI1, MEN1, MET, MITF, MLH1, MLH3, MRE11, MSH2, Elemental Analysis
Alpha 1-Antitrypsin-Mangel Alpha-1-Antitrypsin-Mangel Elemental Analysis
BRCA-Panel; BRCA1, BRCA2 BRCA-Panel; BRCA1, BRCA2 Elemental Analysis
GLA; Morbus Fabry GLA; Morbus Fabry Elemental Analysis
Genetikum-Panel Genetikum-Panel Elemental Analysis
HFE Hämochromatose --HFE Elemental Analysis
Markerchromosomen-Abklärung Markerchromosomen-Abklärung Elemental Analysis
Mikrodeletions- und Mikrodeletions- und Elemental Analysis
Mikroduplikationssyndrome Mikroduplikationssyndrome Elemental Analysis
NOBOX, NR5A1, NRAS, NSD1, NTHL1, PADI6, PALB2, PANX1, PATL2, PBRM1, PCSK9, PDGFRA, PHOX2B, PIK3CA, PIK3R2, PKP2, PMS1, PMS2, POF1B, POLD1, POLE, POR, POT1, POU6F2, PRKAG2, PRKAR1A, PRSS1, PTCH1, PTCH2, PTEN, PTPN11, RAD21, RAD50, RAD51, RAD51B, RAD51C, RAD51D, RASA1, RASA2, RB1, REC114, RECQL4, REST, RET, RHBDF2, RINT1, RNF43, RUNX1, RYR1, RYR2, SCN4A, SCN5A, SDHA, SDHAF2, SDHB, SDHC, SDHD, SEC23B, SHOC1, SLC35A2, SLX4, SMAD3, SMAD4, SMARCA4, SMARCB1, SMARCC2, SMARCD1, SMARCE1, SMC1A, SMC3, SOX11, SOX4, SPINK1, SPRED1, STAG3, STAR, STK11, SUFU, SYCE1, SYCP2, TERC, TERF2IP, TERT, TEX11, TEX14, TEX15, TGFBR1, TGFBR2, TLE6, TMEM127, TMEM43, TNNI3, TNNT2, TP53, TPM1, TRIP13, TSC1, TSC2, TUBB8, VHL, WEE2, WRN, NOBOX, NR5A1, NRAS, NSD1, NTHL1, PADI6, PALB2, PANX1, PATL2, PBRM1, PCSK9, PDGFRA, PHOX2B, PIK3CA, PIK3R2, PKP2, PMS1, PMS2, POF1B, POLD1, POLE, POR, POT1, POU6F2, PRKAG2, PRKAR1A, PRSS1, PTCH1, PTCH2, PTEN, PTPN11, RAD21, RAD50, RAD51, RAD51B, RAD51C, RAD51D, RASA1, RASA2, RB1, REC114, RECQL4, REST, RET, RHBDF2, RINT1, RNF43, RUNX1, RYR1, RYR2, SCN4A, SCN5A, SDHA, SDHAF2, SDHB, SDHC, SDHD, SEC23B, SHOC1, SLC35A2, SLX4, SMAD3, SMAD4, SMARCA4, SMARCB1, SMARCC2, SMARCD1, SMARCE1, SMC1A, SMC3, SOX11, SOX4, SPINK1, SPRED1, STAG3, STAR, STK11, SUFU, SYCE1, SYCP2, TERC, TERF2IP, TERT, TEX11, TEX14, TEX15, TGFBR1, TGFBR2, TLE6, TMEM127, TMEM43, TNNI3, TNNT2, TP53, TPM1, TRIP13, TSC1, TSC2, TUBB8, VHL, WEE2, WRN, Elemental Analysis
PTPN11 PTPN11 Elemental Analysis
Subtelomeranalyse Subtelomeranalyse Elemental Analysis
WT1, XPA, XPC, XRCC2, XRCC3, ZP2, ZP3 WT1, XPA, XPC, XRCC2, XRCC3, ZP2, ZP3 Elemental Analysis
Whole Exome Sequenzierung (WES) Whole Exome Sequenzierung (WES) Elemental Analysis
(GLUT1) (GLUT1) Molecular Diagnostics / PCR
(Typ Kennedy) (Typ Kennedy) Molecular Diagnostics / PCR
ADCY5, PNKD, PRRT2, SLC2A1 ADCY5, PNKD, PRRT2, SLC2A1 Molecular Diagnostics / PCR
Adrenogenitales Syndrom (AGS) Adrenogenitales-Syndrom (AGS) Molecular Diagnostics / PCR
Angelman Syndrom Deletion; Angelman-Syndrom Molecular Diagnostics / PCR
Atrophie Spinobulbäre Muskelatrophie Molecular Diagnostics / PCR
BRCA1 BRCA1 Molecular Diagnostics / PCR
Brust- und Eierstockkrebs Familiärer Brust- und Eierstockkrebs Molecular Diagnostics / PCR
CYP21A2 CYP21A2 Molecular Diagnostics / PCR
Chorea Huntington HD; Chorea Huntington Molecular Diagnostics / PCR
Chorea Huntington (HD)-HTT Chorea Huntington (HD)-HTT Molecular Diagnostics / PCR
Cystische Fibrose Cystische Fibrose: Screening der Molecular Diagnostics / PCR
Ethanolamin, Fortsetzung Ethanolamin, Fortsetzung Molecular Diagnostics / PCR
FGFR3 OMIM*176943, FGFR3 Molecular Diagnostics / PCR
GJB2 syndromale (DFNB1) [GJB2 Molecular Diagnostics / PCR
Glukose-Transporter-Defizienz Glukose-Transporter-Defizienz Molecular Diagnostics / PCR
Hereditäre Neuropathie mit Hereditäre Neuropathie mit Molecular Diagnostics / PCR
LEOPARD-Syndrom (LPRD1) LEOPARD-Syndrom (LPRD1) Molecular Diagnostics / PCR
MECP2 MECP2 Molecular Diagnostics / PCR
Markeranalyse STR-Markeranalyse Molecular Diagnostics / PCR
MeCP2; Rett-Syndrom MeCP2; Rett-Syndrom Molecular Diagnostics / PCR
PMP22 PMP22 Molecular Diagnostics / PCR
Prader Willi Syndrom Prader-Willi-Syndrom: Molecular Diagnostics / PCR
SHOX-Defizienz SHOX-Defizienz: Leri-Weill- Molecular Diagnostics / PCR
Smith-Lemli-Opitz-Syndrom (SLOS) Smith-Lemli-Opitz-Syndrom (SLOS) Molecular Diagnostics / PCR
Spinale Muskelatrophie (SMA) Spinale Muskelatrophie (SMA): Molecular Diagnostics / PCR
UBE3A UBE3A Molecular Diagnostics / PCR
Alpha-1-Antitrypsin (SERPINA1- Alpha-1-Antitrypsin (SERPINA1- Other
DHCR7 Smith-Lemli-Opitz-Syndrom (DHCR7 Other
DMD Muskeldystrophie Becker (DMD Other
DMPK DMPK Other
FMR1 Tremor-Ataxie-Syndrom (FMR1 Other
GAA GAA Other
GLA GLA Other
Morbus Meulengracht (UGT1A1 Morbus Meulengracht (UGT1A1 Other
SHOX SHOX Other
Syndrom), Crigler-Najjar-Syndrom Syndrom), Crigler-Najjar-Syndrom Other
Azoospermiefaktor Azoospermiefaktor Sterility Testing
SMN1 SMN1 Sterility Testing
*) 1 bar; 2 bar *) 1 bar; 2 bar Temperature / Pressure
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