Orphanet: SYNLAB Medizinisches Versorgungszentrum Humane Genetik M�nchen
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SYNLAB Medizinisches Versorgungszentrum Humane Genetik München

  • Zweigniederlassung der SYNLAB MVZ Augsburg GmbH
  • Lindwurmstr. 23
  • 80337 MÜNCHEN
  • ALEMANHA
  • Estado : Privado com fins lucrativos
  • Contacto telefónico : 49 (0)89 548629 0
  • Contacto telefónico adicional : -
  • Fax : 49 (0)89 548629 243
  • Website
  • Contacto
  • Número EUGT : EUGTDE41863

Gestão da qualidade

Acreditação Acreditação

Acreditação
Organismo
Ano
Alcance de la acreditación

EQA EQA

Esquema(s) de EQA organizado(s) por CEQAS

Amniotic Fluid
2015, 2016, 2017
Bloods - Postnatal
2015, 2016, 2017
CVS
2015, 2016, 2017
Constitutional microarray (postnatal)
2015, 2016, 2017
FISH PGD (Blastomere)
2016
PGD Blastomere/Trophectoderm array/NGS for aneuploidy pilot
2016, 2017
PGD Blastomere/Trophectoderm array/NGS for translocations pilot
2016, 2017
Pilot PGD microarray blastomere/trophectoderm
2015
Pilot Products of conception (Array/MLPA/PCR)
2015
Prenatal array exploratory pilot and survey
2015
Prenatal microarray
2016, 2017
Products of conception
2015
Products of conception (Array/MLPA/QF-PCR/NGS)
2016, 2017
Products of conception (G-banding)
2016, 2017
Rapid aneuploidy FISH
2015, 2016, 2017

Esquema(s) de EQA organizado(s) por CF Network

CF (Cystic fibrosis)
2015, 2016

Esquema(s) de EQA organizado(s) por EMQN

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

Esquema(s) de EQA organizado(s) por GenQA

Amniotic Fluid
2018
Bloods - Postnatal
2018
CF (Cystic fibrosis)
2018
Chorionic Villus
2018
Constitutional microarray (postnatal)
2018
Fabry disease
2018
Preimplantation Genetic Testing by NGS and/or arrays for trophectoderm and/or blastomere testing for chromosomal rearrangements
2018
Preimplantation Genetic Testing for monogenic disorders Stage 1
2018
Preimplantation Genetic Testing for monogenic disorders Stage 2
2018
Preimplantation Genetic Testing of Trophectoderm and/or Blastomere for aneuploidies by NGS and/or arrays
2018
Prenatal constitutional CNV detection
2018
Products of Conception/Fetal tissue (Molecular methods)
2018
Products of conception (G-banding)
2018
Rapid Prenatal Aneuploidy FISH
2018
Os documentos contidos neste website são apresentação para efeitos apenas de informação. O material não substitui os cuidados médicos profissinais por um especialista profissional qualificado e não deve ser usado como base para diagnóstico ou tratamento.