ScopeMVZ der Universitätsmedizin Mainz GmbH Fachgebiet Humangenetik, molekulargenetisches Labor
105 capabilities
Accredited since September 2025
Verified Apr 2026
One of 3,039 in Germany
Details
Langenbeckstraße 1
Mainz 55131 , Germany
Mainz 55131 , Germany
Accreditation
Active
DAkkS
D-ML-21458-02-01
Specialises in molecular and cytogenetic human genetics testing including chromosomal analysis using SNP arrays and sequencing-based methods for copy-number variation detection on blood and tissue samples.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-21458-02-01
Status
ActiveSince
04 September 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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Test Capabilities (105)
| Standard Reference | Description | Category |
|---|---|---|
| Angeborener Chromosomensatz | angeborener Chromosomensatz | Biocompatibility (ISO 10993) |
| BRCA-Panel; BRCA1, BRCA2 | BRCA-Panel; BRCA1, BRCA2 | Elemental Analysis |
| Brust- u. Ovarialkrebs, hereditär | Brust- u. Ovarialkrebs, hereditär | Elemental Analysis |
| H19, KCNQ1OT1 | H19, KCNQ1OT1 | Elemental Analysis |
| PTPN11 | PTPN11 | Elemental Analysis |
| Silver-Russell Syndrom | Silver-Russell-Syndrom: | Elemental Analysis |
| (G11778A) und MTND6P (T14484C) | (G11778A) und MTND6P (T14484C) | Molecular Diagnostics / PCR |
| (GUSB ) | (GUSB ) | Molecular Diagnostics / PCR |
| (HSP): ATL1 | REEP1, SPG7 (HSP) | Molecular Diagnostics / PCR |
| (NAGLU ); Typ IV B (GLB1 ); Typ | (NAGLU ); Typ IV B (GLB1 ); Typ | Molecular Diagnostics / PCR |
| (patUPD14) - | (patUPD14): | Molecular Diagnostics / PCR |
| APC, CDKN2A, EPCAM, MLH1, MSH2, MSH6, PMS2, POLD1, POLE,PTCH1, SMARCE1, SUFU, TP53, NF1, NF2, TSC1, TSC2 | APC, CDKN2A, EPCAM, MLH1, MSH2, MSH6, PMS2, POLD1, POLE,PTCH1, SMARCE1, SUFU, TP53, NF1, NF2, TSC1, TSC2 | Molecular Diagnostics / PCR |
| APC2, NFIX, NSD1 | APC2, NFIX, NSD1 | Molecular Diagnostics / PCR |
| Aicardi-Goutières Syndrom | Aicardi-Goutières-Syndrom | Molecular Diagnostics / PCR |
| Alzheimer/Demenz: | Alzheimer/Demenz: | Molecular Diagnostics / PCR |
| Angeborener Herzfehler Typ 6: | Angeborener Herzfehler Typ 6: | Molecular Diagnostics / PCR |
| Angelman Syndrom | Deletion; Angelman-Syndrom | Molecular Diagnostics / PCR |
| Aniridie: | Aniridie: | Molecular Diagnostics / PCR |
| Ataxie-Syndrom (FXTAS); Fragiles | Ataxie-Syndrom (FXTAS); Fragiles | Molecular Diagnostics / PCR |
| Autosomal dominante polyzystische | Autosomal dominante polyzystische | Molecular Diagnostics / PCR |
| Beckwith-Wiedemann Syndrom | Beckwith-Wiedemann-Syndrom: | Molecular Diagnostics / PCR |
| CFHR5 | CFHR5 | Molecular Diagnostics / PCR |
| CHEK2, TP53 | CHEK2, TP53 | Molecular Diagnostics / PCR |
| CMT1A, HNPP: | CMT1A, HNPP: | Molecular Diagnostics / PCR |
| CREBBP, EP300 | CREBBP, EP300 | Molecular Diagnostics / PCR |
| Chorea Huntington (HD)-HTT | Chorea Huntington (HD)-HTT | Molecular Diagnostics / PCR |
| Crigler-Najjar-Syndrom | Crigler-Najjar-Syndrom | Molecular Diagnostics / PCR |
| DiGeorge-Syndrom (22q11.2) | DiGeorge-Syndrom (22q11.2) | Molecular Diagnostics / PCR |
| Differentialdiagnosen: SCN1A | Myopie und Differentialdiagnosen: | Molecular Diagnostics / PCR |
| Dravet-Syndrom und | Dravet-Syndrom und | Molecular Diagnostics / PCR |
| Duchenne/Becker: | Typ Duchenne/Becker | Molecular Diagnostics / PCR |
| Episoden | Episoden | Molecular Diagnostics / PCR |
| F2: dbSNP rs1799963 | SMARCB1, LZTR1, NF2 | Molecular Diagnostics / PCR |
| FBN1 | FBN1 | Molecular Diagnostics / PCR |
| GDF1 | GDF1 | Molecular Diagnostics / PCR |
| GJB2, GJB6 | GJB2, GJB6 | Molecular Diagnostics / PCR |
| GJB6, STRC, OTOA | GJB6, STRC, OTOA | Molecular Diagnostics / PCR |
| GRB10 | GRB10 | Molecular Diagnostics / PCR |
| Gorlin-Goltz-Syndrom | Gorlin-Goltz-Syndrom: | Molecular Diagnostics / PCR |
| H19, LIT1 | H19, LIT1 | Molecular Diagnostics / PCR |
| H19, MEST | H19, MEST | Molecular Diagnostics / PCR |
| Hereditäre Schwannomatose | Hereditäre Schwannomatose | Molecular Diagnostics / PCR |
| Hereditäre spastische Paraplegie | Hereditäre spastische Paraplegie | Molecular Diagnostics / PCR |
| Holoprosenzephalie | Holoprosenzephalie | Molecular Diagnostics / PCR |
| Idiopathischer Kleinwuchs: | Idiopathischer Kleinwuchs: | Molecular Diagnostics / PCR |
| KRAS; Noonan-Syndrom | KRAS; Noonan-Syndrom | Molecular Diagnostics / PCR |
| Kagami-Ogata Syndrom | Kagami-Ogata-Syndrom | Molecular Diagnostics / PCR |
| Komplementdefekte (Neisseria): | Komplementdefekte (Neisseria): | Molecular Diagnostics / PCR |
| Li Fraumeni Syndrom | Li-Fraumeni-Syndrom | Molecular Diagnostics / PCR |
| Lissenzephalie | Lissenzephalie | Molecular Diagnostics / PCR |
| MECP2 | MECP2 | Molecular Diagnostics / PCR |
| MECP2 -Duplikationssyndrom | MECP2 -Duplikationssyndrom | Molecular Diagnostics / PCR |
| MEG3 | MEG3 | Molecular Diagnostics / PCR |
| MID1 | MID1 | Molecular Diagnostics / PCR |
| MTND1P (G3460A), MTND4P | MTND1P (G3460A), MTND4P | Molecular Diagnostics / PCR |
| MTRNR1 | MTRNR1 | Molecular Diagnostics / PCR |
| Marfan Syndrom | Marfan-Syndrom: FBN1, TGFBR1, TGFBR2, ACTA2, COL3A1, MYH11, MYLK, SMAD3, TGFB2 | Molecular Diagnostics / PCR |
| Maternal vererbter Diabetes | Maternal vererbter Diabetes | Molecular Diagnostics / PCR |
| MeCP2; Rett-Syndrom | MeCP2; Rett-Syndrom | Molecular Diagnostics / PCR |
| Mikrodeletionsscreening | Mikrodeletionsscreening | Molecular Diagnostics / PCR |
| Mukopolysaccharidosen TypI | Mukopolysaccharidosen TypI | Molecular Diagnostics / PCR |
| Muskelatrophie Typ Kennedy | Muskelatrophie Typ Kennedy | Molecular Diagnostics / PCR |
| Mütterliche Kontamination (STR) | Mütterliche Kontamination (STR) | Molecular Diagnostics / PCR |
| NF1, NF2, SPRED1 | NF1, NF2, SPRED1 | Molecular Diagnostics / PCR |
| NF1; V. a. Neurofibromatose | NF1; V. a. Neurofibromatose | Molecular Diagnostics / PCR |
| NSD1; Sotos-Syndrom | NSD1; Sotos-Syndrom | Molecular Diagnostics / PCR |
| Neuralrohrdefekte: | Neuralrohrdefekte: | Molecular Diagnostics / PCR |
| Nierenerkrankung (ADPKD) | Nierenerkrankung (ADPKD): PKD1, | Molecular Diagnostics / PCR |
| Opitz-Syndrom: | Smith-Lemli-Opitz-Syndrom | Molecular Diagnostics / PCR |
| PAX6 | PAX6 | Molecular Diagnostics / PCR |
| PKD2 | PKD2 | Molecular Diagnostics / PCR |
| PMP22 | PMP22 | Molecular Diagnostics / PCR |
| PRKN, PINK1, SNCAM | PRKN, PINK1, SNCAM | Molecular Diagnostics / PCR |
| PTCH1 | PTCH1 | Molecular Diagnostics / PCR |
| Parkinson | Parkinson: | Molecular Diagnostics / PCR |
| Prader Willi Syndrom | Prader-Willi-Syndrom: | Molecular Diagnostics / PCR |
| Repeat-Analyse Chorea Huntington: | Repeat-Analyse Chorea Huntington: | Molecular Diagnostics / PCR |
| Repeatanalyse: | Repeatanalyse: | Molecular Diagnostics / PCR |
| Rett-Syndrom Sequenzierung: | Rett-Syndrom Sequenzierung: | Molecular Diagnostics / PCR |
| Rubinstein-Taybi Syndrom | Rubinstein-Taybi-Syndrom: | Molecular Diagnostics / PCR |
| SHH, ZIC2, SIX3, GLI2, TGIF1 | SHH, ZIC2, SIX3, GLI2, TGIF1 | Molecular Diagnostics / PCR |
| SMN1, SMN2 | SMN1, SMN2 | Molecular Diagnostics / PCR |
| SMN1; Spinale Muskelatrophie | SMN1; Spinale Muskelatrophie | Molecular Diagnostics / PCR |
| Schwerhörigkeit, mitochondrial: | Schwerhörigkeit, mitochondrial: | Molecular Diagnostics / PCR |
| Schwerhörigkeit, nicht syndromal | Schwerhörigkeit, nicht-syndromal: | Molecular Diagnostics / PCR |
| Spingolipidosen Typ 2 (HEXB ) | Spingolipidosen Typ 2 (HEXB ) | Molecular Diagnostics / PCR |
| Subtelomerscreening | Subtelomerscreening | Molecular Diagnostics / PCR |
| TREX1, SAMHD1 | TREX1, SAMHD1 | Molecular Diagnostics / PCR |
| Tuberöse Sklerose | Tuberöse Sklerose: TSC1, | Molecular Diagnostics / PCR |
| UBE3A | UBE3A | Molecular Diagnostics / PCR |
| VANGL1, VANGL2 | VANGL1, VANGL2 | Molecular Diagnostics / PCR |
| Whole Exome Sequencing | Whole Exome Sequencing | Molecular Diagnostics / PCR |
| X-Inaktivierungstatus (HUMARA) | X-Inaktivierungstatus (HUMARA) | Molecular Diagnostics / PCR |
| mellitus mit Schwerhörigkeit | mellitus mit Schwerhörigkeit | Molecular Diagnostics / PCR |
| schwere Oligozoospermie: | schwere Oligozoospermie: | Molecular Diagnostics / PCR |
| APP | APP | Other |
| DMD | Muskeldystrophie Becker (DMD | Other |
| DMD (Muskeldystrophie Typ | DMD (Muskeldystrophie Typ | Other |
| FMR1 | Tremor-Ataxie-Syndrom (FMR1 | Other |
| MEST | MEST | Other |
| Morbus Meulengracht (UGT1A1 | Morbus Meulengracht (UGT1A1 | Other |
| SHOX | SHOX | Other |
| Spots: | Spots: | Other |
| Synrom: | Synrom: | Other |
| *) 1 bar; 2 bar | *) 1 bar; 2 bar | Temperature / Pressure |