Orphanet: MVZ Dr. Eberhard und Partner Bereich Laboratoriumsmedizin und Humangenetik
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MVZ Dr. Eberhard und Partner - Bereich Laboratoriumsmedizin und Humangenetik

  • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
  • Brauhausstra▀e 4
  • 44137 DORTMUND
  • GERMANY
  • Status : Private for-profit
  • Phone : 49 (0)231 95720
  • Additional Phone : -
  • Fax : 49 (0)231 553619
  • Website
  • Contact
  • EUGT number : EUGTDE40555

Quality management

Accreditation
 Accreditation

Accreditation
Organism
Year
Accreditation scope

EQA
 EQA

EQA scheme(s) organized by CF Network

CF (Cystic fibrosis)
2015, 2016, 2017, 2018, 2019

EQA scheme(s) organized by EMQN

11p-Imprinting Disorder Scheme (BWS/SRS)
2016, 2017, 2018, 2019
ADPKD (Adult dominant polycystic kidney disease)
2016, 2017, 2019
AZF (Y-Chromosome microdeletions)
2019
CAH (Congenital Adrenal Hyperplasia)
2018, 2019
CMT/HNPP (Charcot-Marie-Tooth disease / Hereditary Neuropathy with Pressure Palsies)
2017, 2018, 2019
Cardiac genetics - Hypertrophic cardiomyopathies
2019
Cardiac genetics - arrthymias
2019
DFNB1 (Hereditary Deafness)
2017, 2018, 2019
DM (Myotonic dystrophy)
2017, 2018, 2019
DMD (Duchenne and Becker muscular dystrophies)
2017, 2018, 2019
EGFR (Molecular testing for non small cell lung cancer)
2017
FAP (Familial Adenomatous Polyposis Colon Cancer)
2017, 2018, 2019
FH (Familial hypercholesterolemia - pilot scheme)
2017, 2018, 2019
FRAX (Fragile X syndrome) - full scheme
2016, 2017, 2018, 2019
FRDA (Friedreich ataxia)
2016, 2017, 2018, 2019
Germline NGS mutation testing
2016, 2017, 2018, 2019
HBOC (Hereditary Breast and Ovarian Cancer testing)
2017, 2018, 2019
HD (Huntington disease)
2016, 2017, 2018, 2019
HFE (Hereditary hemochromatosis)
2017, 2018, 2019
HNPCC (Hereditary non-polyposis colon cancer)
2017, 2018, 2019
HRF (Hereditary Recurrent Fevers)
2017, 2018, 2019
MEN2 (Multiple Endocrine Neoplasia Type 2)
2017, 2018, 2019
Mitochondrial metabolic disorders
2017, 2018, 2019
Molecular testing of somatic changes in BRCA genes for ovarian cancer
2018
MonoDiab (Monogenic Diabetes)
2017, 2018, 2019
OI (Osteogenesis imperfecta)
2017, 2018, 2019
ONCOPANEL (Oncogene panel testing) - pilot scheme
2016, 2017, 2019
PKU (Phenylketonuria)
2017, 2018, 2019
POR (Porphyria)
2017, 2018, 2019
PWAS (Prader-Willi and Angelman syndromes)
2017, 2018, 2019
RYR1 related disorders
2019
SCA (Spinocerebellar ataxias)
2017, 2018, 2019
SEQ (DNA sequencing) - Full scheme
2018, 2019
SHOX (Short stature homeobox gene testing)
2017, 2018, 2019
SMA (Spinal muscular atrophy)
2017, 2018, 2019
Somatic NGS mutation testing
2017, 2019
Stickler syndrome
2019
VHL (Von Hippel Lindau syndrome)
2017, 2018, 2019
WIL (Wilson disease)
2017, 2018, 2019
aCGH/ Microarrays
2016, 2017, 2018, 2019

EQA scheme(s) organized by GenQA

Fabry disease
2018
MCADD
2018
cfDNA testing in lung cancer pilot
2018
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.