ScopeUniversitätsklinikum Heidelberg Institut für Humangenetik
49 capabilities
Accredited since April 2025
Verified May 2026
One of 3,188 in Germany
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Details
Im Neuenheimer Feld 366
Heidelberg 69120 , Germany
Heidelberg 69120 , Germany
Accreditation
Active
DAkkS
D-ML-13060-03-00
Specialises in molecular and cytogenetic human genetics testing with flexible accreditation permitting procedure modification and development. Testing focuses on DNA-based molecular diagnostics including PCR analysis of fragile X syndrome and related genetic conditions from blood and saliva samples.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-13060-03-00
Status
ActiveSince
03 April 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 (49)
| Standard Reference | Description | Category |
|---|---|---|
| Angeborener Chromosomensatz | angeborener Chromosomensatz | Biocompatibility (ISO 10993) |
| Erworbener Chromosomensatz | erworbener Chromosomensatz | Biocompatibility (ISO 10993) |
| - Oberschalenwaagen | - Oberschalenwaagen | Force / Torque |
| SR | körpers r | Hardness (Vickers, Rockwell, Brinell) |
| (ACVRL1 (ALK1 ), BMPR2 und ENG) | (ACVRL1 (ALK1 ), BMPR2 und ENG) | Molecular Diagnostics / PCR |
| (ALK1 ), BMPR2, ENG , GDF2 | (ALK1 ), BMPR2, ENG , GDF2 | Molecular Diagnostics / PCR |
| (APC -Gen) | (APC -Gen) | Molecular Diagnostics / PCR |
| (BRCA1-, BRCA2- Gen) | (BRCA1-, BRCA2- Gen) | Molecular Diagnostics / PCR |
| (CFTR-Gen) | Erkrankungen (CFTR -Gen) | Molecular Diagnostics / PCR |
| (CYP21A2- Gen) | (CYP21A2- Gen) | Molecular Diagnostics / PCR |
| (EIF2AK4 ) | (EIF2AK4 ) | Molecular Diagnostics / PCR |
| (HTT-Gen) | Huntington-Erkrankung (HTT -Gen) | Molecular Diagnostics / PCR |
| (OTC -Gen) | (OTC -Gen) | Molecular Diagnostics / PCR |
| 5-Fluorouracil Unverträglichkeit: | 5-Fluorouracil Unverträglichkeit: | Molecular Diagnostics / PCR |
| Abklärung einer bekannten | Abklärung einer bekannten | Molecular Diagnostics / PCR |
| Adenomatöse Polyposis | Familiäre Adenomatöse Polyposis | Molecular Diagnostics / PCR |
| Adrenogenitales Syndrom | Adrenogenitales Syndrom | Molecular Diagnostics / PCR |
| Autosomale Rezessive | Autosomale Rezessive | Molecular Diagnostics / PCR |
| Brust- und Eierstockkrebs | Familiärer Brust- und Eierstockkrebs | Molecular Diagnostics / PCR |
| Cystische Fibrose, CFTR -assoziierte | Cystische Fibrose, CFTR -assoziierte | Molecular Diagnostics / PCR |
| Familiäre monogene Erkrankung | Familiäre monogene Erkrankung | Molecular Diagnostics / PCR |
| Fragiles X-Syndrom, primäre | Fragiles X-Syndrom, primäre | Molecular Diagnostics / PCR |
| Glutarazidurie Typ 1 (GCDH -Gen) | Glutarazidurie Typ 1 (GCDH -Gen) | Molecular Diagnostics / PCR |
| Indirekte Diagnostik | Indirekte Diagnostik | Molecular Diagnostics / PCR |
| Mangel | Ornithin-Transcarbamylase-Mangel | Molecular Diagnostics / PCR |
| Osler-Rendu-Weber Syndrom | Osler-Rendu-Weber Syndrom | Molecular Diagnostics / PCR |
| PGT-M | PGT-M | Molecular Diagnostics / PCR |
| Phenylketonurie (PAH -Gen) | Phenylketonurie (PAH -Gen) | Molecular Diagnostics / PCR |
| Pulmonal-arterielle Hpyertonie | Pulmonal-arterielle Hpyertonie | Molecular Diagnostics / PCR |
| familiären | familiären | Molecular Diagnostics / PCR |
| veno-okklusive Erkrankung | veno-okklusive Erkrankung | Molecular Diagnostics / PCR |
| (BMP9 ) und SMAD4 ); Pulmonal | (BMP9 ) und SMAD4 ); Pulmonal | Other |
| (Haplotypanalyse, maternaler | (Haplotypanalyse, maternaler | Other |
| , RAD51D-, CHEK2-, PALB2-, ATM-, BRIP1-, CDH1- und TP53 -Gen) | , RAD51D-, CHEK2-, PALB2-, ATM-, BRIP1-, CDH1- und TP53 -Gen) | Other |
| 11q13 | Angelman-Syndrom (15q11-q13 | Other |
| APOA1 - und FGA -Gen) | APOA1 - und FGA -Gen) | Other |
| Adenomatöse Polyposis (MUTYH | Adenomatöse Polyposis (MUTYH | Other |
| DHCR7 | Smith-Lemli-Opitz-Syndrom (DHCR7 | Other |
| DMD | Muskeldystrophie Becker (DMD | Other |
| Dehydrogenase-Mangel (ACADM | Dehydrogenase-Mangel (ACADM | Other |
| Erkrankungen (ELUCIGENE™ CF-EU2 | Erkrankungen (ELUCIGENE™ CF-EU2 | Other |
| FMR1 | Tremor-Ataxie-Syndrom (FMR1 | Other |
| Gen) | Parietalzellen/Magen) | Other |
| Kit; CFTR -Gen) | Kit; CFTR -Gen) | Other |
| Kontaminationsausschluss, Uniparentale Disomie 7/14/15/X) | Kontaminationsausschluss, Uniparentale Disomie 7/14/15/X) | Other |
| Prader-Willi-Syndrom (15q11-q13 | Prader-Willi-Syndrom (15q11-q13 | Other |
| Region) | Region) | Other |
| Rendu-Weber Syndrom (ACVRL1 | Rendu-Weber Syndrom (ACVRL1 | Other |
| partieller Chromosomensatz (zur | partieller Chromosomensatz (zur | Other |
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