Universitätsklinikum Heidelberg Institut für Humangenetik

49 capabilities Accredited since April 2025 Verified Apr 2026 One of 3,039 in Germany

Details

Im Neuenheimer Feld 366
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

Active

Since

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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49 capabilities

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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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