ScopeMedizinisches Versorgungszentrum am Universitätsklinikum Carl Gustav Carus Dresden GmbH Fachbereich Humangenetik
65 capabilities
Accredited since December 2024
Verified May 2026
One of 3,188 in Germany
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Details
Fetscherstr. 74
Dresden 01307 , Germany
Dresden 01307 , Germany
Accreditation
Active
DAkkS
D-ML-13245-01-01
Provides human genetic testing in cytogenetics and molecular human genetics, including PCR-based amplification techniques and DNA sequencing methods such as Sanger sequencing and capillary gel electrophoresis.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-13245-01-01
Status
ActiveSince
20 December 2024
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 (65)
| Standard Reference | Description | Category |
|---|---|---|
| Angeborener Chromosomensatz | angeborener Chromosomensatz | Biocompatibility (ISO 10993) |
| MCAD-Mangel (OMIM 201450) | MCAD-Mangel (OMIM 201450) | Chromatography (GC, HPLC) |
| Phenylketonurie (OMIM 261600) | Phenylketonurie (OMIM 261600) | Chromatography (GC, HPLC) |
| Psoriasis pustulosa (OMIM 614204) | Psoriasis pustulosa (OMIM 614204) | Chromatography (GC, HPLC) |
| STING-assoziierte Vaskulopathie | STING-assoziierte Vaskulopathie | Chromatography (GC, HPLC) |
| Spondyloenchondrodysplasia | Spondyloenchondrodysplasia | Chromatography (GC, HPLC) |
| (AAAS) | (AAAS) | Molecular Diagnostics / PCR |
| (ACADM) | (ACADM) | Molecular Diagnostics / PCR |
| (CFTR) | (CFTR) | Molecular Diagnostics / PCR |
| (IL36RN) | (IL36RN) | Molecular Diagnostics / PCR |
| (NLRP3) | Syndrome (NLRP3) | Molecular Diagnostics / PCR |
| (OMIM 231550) (GMPPA) | (OMIM 231550) (GMPPA) | Molecular Diagnostics / PCR |
| (OMIM 613399, 614291, 612555) | (OMIM 613399, 614291, 612555) | Molecular Diagnostics / PCR |
| (OMIM 615510), Triple-A-Syndroms | (OMIM 615510), Triple-A-Syndroms | Molecular Diagnostics / PCR |
| (PAH) | (PAH) | Molecular Diagnostics / PCR |
| (SAVI; OMIM 615934), Chilblain | (SAVI; OMIM 615934), Chilblain | Molecular Diagnostics / PCR |
| (TNFRSF1A) | Syndrom (TNFRSF1A) | Molecular Diagnostics / PCR |
| 225750), Chilblain Lupus (OMIM | 225750), Chilblain Lupus (OMIM | Molecular Diagnostics / PCR |
| 615688), Sneddon Syndrom (OMIM | 615688), Sneddon Syndrom (OMIM | Molecular Diagnostics / PCR |
| Alakrimie-Achalasie-Mentale | Alakrimie-Achalasie-Mentale | Molecular Diagnostics / PCR |
| Ausschlusstest Fragiles X-Syndrom | Ausschlusstest Fragiles X-Syndrom | Molecular Diagnostics / PCR |
| CNV-Detektion, genomweit | CNV-Detektion, genomweit | Molecular Diagnostics / PCR |
| Chromosomen 13, 18, 21, X und | Chromosomen 13, 18, 21, X und | Molecular Diagnostics / PCR |
| Cryopyrin associated periodic fever | Cryopyrin associated periodic fever | Molecular Diagnostics / PCR |
| Cystic Fibrosis (CF, OMIM 219700) | Cystic Fibrosis (CF, OMIM 219700) | Molecular Diagnostics / PCR |
| Eierstockkrebs (ATM, BRCA1, BRCA2, CDH1, CHEK2, PALB2, RAD51C, RAD51D, TP53, BRIP1) | Eierstockkrebs (ATM, BRCA1, BRCA2, CDH1, CHEK2, PALB2, RAD51C, RAD51D, TP53, BRIP1) | Molecular Diagnostics / PCR |
| HNPCC (Lynch-syndrom) (MLH1, MSH2, MSH6, APC, PSM2, MUTYH, CDH1) (OMIM 614385, 614350, 614337, 614331, 613244, 609310) | HNPCC (Lynch-syndrom)(MLH1, MSH2, MSH6, APC, PSM2, MUTYH, CDH1) (OMIM 614385, 614350, 614337, 614331, 613244, 609310) | Molecular Diagnostics / PCR |
| Hereditärer Brust- und | Hereditärer Brust- und | Molecular Diagnostics / PCR |
| ICE-fever (CASP1) | ICE-fever (CASP1) | Molecular Diagnostics / PCR |
| Lupus (OMIM 610448) (TMEM173) | Lupus (OMIM 610448) (TMEM173) | Molecular Diagnostics / PCR |
| Nummerische Veränderungen | Nummerische Veränderungen | Molecular Diagnostics / PCR |
| Repeatanlyse FMR1 | Repeatanlyse FMR1 | Molecular Diagnostics / PCR |
| Retardierung (AAMR)-Syndrom | Retardierung (AAMR)-Syndrom | Molecular Diagnostics / PCR |
| Syndrom (OMIM 182250) (IFIH1) | Syndrom (OMIM 182250) (IFIH1) | Molecular Diagnostics / PCR |
| Triple-A-syndrom (OMIM 231550) | Triple-A-syndrom (OMIM 231550) | Molecular Diagnostics / PCR |
| Tumor necrosis factor alpha | Tumor necrosis factor alpha | Molecular Diagnostics / PCR |
| Whole Exome Sequencing | Whole Exome Sequencing | Molecular Diagnostics / PCR |
| Whole Genome Sequencing; SNV, CNV | Whole Genome Sequencing; SNV, CNV | Molecular Diagnostics / PCR |
| chromosomaler/numerischer | chromosomaler/numerischer | Molecular Diagnostics / PCR |
| gezielte Variantentestung | gezielte Variantentestung | Molecular Diagnostics / PCR |
| ldentifizierung kleinster | ldentifizierung kleinster | Molecular Diagnostics / PCR |
| receptor associated periodic fever | receptor associated periodic fever | Molecular Diagnostics / PCR |
| syndrome (CAPS, OMIM 606416) | syndrome (CAPS, OMIM 606416) | Molecular Diagnostics / PCR |
| syndrome (TRAPS, OMIM 191190) | syndrome (TRAPS, OMIM 191190) | Molecular Diagnostics / PCR |
| veränderter Chromosomen | veränderter Chromosomen | Molecular Diagnostics / PCR |
| 143890) (LDLR) | 143890) (LDLR) | Other |
| 143890) (PCSK9) | 143890) (PCSK9) | Other |
| 182410) (CECR1) | 182410) (CECR1) | Other |
| 607944) (ACP5) | 607944) (ACP5) | Other |
| 610329) (RNASEH2A) | 610329) (RNASEH2A) | Other |
| 610329) (RNASEH2C) | 610329) (RNASEH2C) | Other |
| 610329) (SAMHD1) | 610329) (SAMHD1) | Other |
| 610448) (TREX1) | 610448) (TREX1) | Other |
| 615010) (ADAR) | 615010) (ADAR) | Other |
| 615846), Singleton-Merten | 615846), Singleton-Merten | Other |
| Aicardi-Goutieres Syndrom (OMIM | Aicardi-Goutieres Syndrom (OMIM | Other |
| Aicardi-Goutieres Syndrom (OMIM1 | Aicardi-Goutieres Syndrom (OMIM1 | Other |
| Aicardi-Goutières Syndrom (OMIM | Aicardi-Goutières Syndrom (OMIM | Other |
| Hypercholesterinämie (OMIM | Hypercholesterinämie (OMIM | Other |
| Polyarteritis nodosa (OMIM | Polyarteritis nodosa (OMIM | Other |
| Septische Granulomatose (chronic | Septische Granulomatose (chronic | Other |
| granulomatous disease, CGD, 300481, 608512) (CYBB) | granulomatous disease, CGD, 300481, 608512) (CYBB) | Other |
| granulomatous disease, CGD, 300481, 608512) (NCF1) | granulomatous disease, CGD, 300481, 608512) (NCF1) | Other |
| lmmundysregulation (OMIM | lmmundysregulation (OMIM | Other |
| varianten) und strukturell | varianten) und strukturell | Other |
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