Medizinisches Versorgungszentrum am Universitätsklinikum Carl Gustav Carus Dresden GmbH Fachbereich Humangenetik

65 capabilities Accredited since December 2024 Verified Apr 2026 One of 3,039 in Germany

Details

Fetscherstr. 74
Dresden 01307 , Germany

Accreditation

Active DAkkS D-ML-13245-01-01
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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

Active

Since

20 December 2024

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

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65 capabilities

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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)
(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
(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
(AAAS) (AAAS) Other
(ACADM) (ACADM) Other
(CFTR) (CFTR) Other
(PAH) (PAH) Other
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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