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FRANCE

PAYS DE LA LOIRE
NANTES

Accreditation
Microscopic polyangiitis: anti-cytoplasm antibodies of neutrophilic polynuclears (ANCA)
CHU de Nantes - Institut de Biologie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

FRANCE

PAYS DE LA LOIRE
NANTES

Accreditation
Granulomatosis with polyangiitis: search for anti-cytoplasm antibodies of neutrophilic polynuclears (ANCA)
CHU de Nantes - Institut de Biologie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

GERMANY

Bayern
MARTINSRIED

Accreditation
Diagnosis of hereditary periodic fever syndromes (NGS screening panel, 14 genes)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

FRANCE

PAYS DE LA LOIRE
NANTES

Accreditation
HLA-A and HLA-B genotyping by PCR SSP or PCR SSO
Etablissement Français du Sang - Pays de Loire
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
SAINT-OUEN-L'AUMÔNE

Accreditation
Diagnosis of susceptibility to Behcet's disease (HLA-B gene)
Laboratoire Cerba
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

HAUTS-DE-FRANCE
LILLE

Accreditation
Diagnosis of susceptibility to Behcet disease (search for HLA-B5 (B51) by PCR-SSO)
CHU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

AUVERGNE-RHONE-ALPES
DÉCINES CHARPIEU

Accreditation
Diagnosis of susceptibility to Behcet disease (HLA-B gene)
Établissement Français du Sang - Auvergne Rhône-Alpes
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of predisposition to Behçet disease (HLA-B gene)
CHU Paris - Hôpital Robert Debré
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation
Diagnosis of susceptibility to Behcet disease (HLA-B gene ; LCT)
Établissement Français du Sang - PACA-Corse
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

AUVERGNE-RHONE-ALPES
LA TRONCHE

Accreditation
Diagnosis of susceptibility to Behcet disease (HLA-B gene: PCR-SSO)
Établissement Français du Sang - Rhône Alpes - Grenoble
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

GERMANY

Bayern
MARTINSRIED

Accreditation
Diagnosis of HLA-B - susceptibility to Behcet's disease, Stevens-Johnson syndrome and ankylosing spondylitis
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

FRANCE

OCCITANIE
MONTPELLIER

Accreditation
Diagnosis of vasculitis due to ADA2 deficiency (CECR1 gene: entire coding region sequencing)
CHU de Montpellier - Hôpital Arnaud de Villeneuve
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, PCR based techniques

FRANCE

BRETAGNE
RENNES

Accreditation
Diagnosis of susceptibility to Behèet disease (HLA-B*51 genotyping)
Établissement Français du Sang - Bretagne
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing, PCR based techniques

GERMANY

Bayern
MÜNCHEN

Accreditation
Diagnosis of vasculitis due to ADA2 deficiency (CECR1 gene)
Medizinisch Genetisches Zentrum München
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Autoinflammatory Disease: Recurrent Fever and Macrophage Activation Syndromes NGS Panel
The Hospital for Sick Children and University of Toronto
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Array based techniques

FRANCE

PAYS DE LA LOIRE
ANGERS

Accreditation
Diagnosis of susceptibility to Behèet disease (HLA-B gene)
Établissement Français du Sang - Angers
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of aplastic anemia (Panel)
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

FRANCE

OCCITANIE
MONTPELLIER

Accreditation
Diagnosis of autoinflammatory diseases (Panel)
CHU de Montpellier - Hôpital Arnaud de Villeneuve
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of autoinflammatory diseases (Panel)
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of interstitial lung disease (Panel)
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing

FRANCE

BRETAGNE
BREST

Accreditation
Diagnosis of susceptibility to Behcet's disease (HLA-B*51:01)
CHU de Brest - Hôpital de la Cavale Blanche
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

AUVERGNE-RHONE-ALPES
LYON

Accreditation
HLA-A and HLA-B genotyping by PCR SSP or PCR SSO
Laboratoire Alpigene
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

GRAND-EST
STRASBOURG

Accreditation
Diagnosis of susceptibility to Behçet disease (HLA-B gene)
Établissement Français du Sang - Grand Est
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

BOURGOGNE-FRANCHE-COMTE
BESANÇON

Accreditation
Diagnosis of susceptibility to Behçet disease (lymphotoxicity and HLA-B genotyping)
Établissement Français du Sang - Bourgogne/Franche-Comté
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Immunology
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of autoinflammatory syndrome of childhood (panel)
Reference Laboratory Genetics
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

FRANCE

AUVERGNE-RHONE-ALPES
LYON

Accreditation
Diagnosis of susceptibility to Behcet's disease (HLA-B and HLA-A genotyping)
Eurofins Biomnis
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

GERMANY

Bayern
MÜNCHEN

Accreditation
Diagnosis of susceptibility to Behcet's disease
Zweigniederlassung der SYNLAB MVZ Augsburg GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

NOUVELLE AQUITAINE
POITIERS

Accreditation
Diagnosis of susceptibility to Behçet disease (HLA-B gene)
Établissement Français du Sang - Poitiers
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

NETHERLANDS

Utrecht
UTRECHT

Accreditation
Molecular diagnosis of Primary Immunodeficiency (gene panel; PID00v17.1)
UMC Utrecht - Universitair Medisch Centrum Utrecht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

NETHERLANDS

Utrecht
UTRECHT

Accreditation
Molecular diagnosis of Autoinflammatory Disease (gene panel; PID01v17.2)
UMC Utrecht - Universitair Medisch Centrum Utrecht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

GERMANY

Bayern
NEU-ULM

Accreditation
Diagnosis of periodic fever syndromes (NGS screening panel: 25 genes)
genetikum - Zweigniederlassung Neu-Ulm
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of STING-associated vasculopathy with onset in infancy (TMEM173 gene)
Reference Laboratory Genetics
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

NETHERLANDS

Gelderland
NIJMEGEN

Accreditation
Diagnosis of STING-associated Vasculopathy with Onset in Infancy (TMEM173 gene)
Radboudumc - Radboud universitair medisch centrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

FRANCE

BRETAGNE
BREST

Accreditation
Diagnosis of susceptibility to uveitis (HLA-B gene)
CHU de Brest - Hôpital de la Cavale Blanche
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

GRAND-EST
VANDOEUVRE-LÈS-NANCY

Accreditation
Diagnosis of vascular disease (Clinical exome)
CHU de Nancy - Hôpitaux de Brabois
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Whole Exome Sequencing (WES)

NETHERLANDS

Limburg
MAASTRICHT

Accreditation
Immunological diagnosis of ANCA-associated Vasculitis (detection of MPO- and PR3-ANCA)
AZM - Academisch Ziekenhuis Maastricht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

NETHERLANDS

Limburg
MAASTRICHT

Accreditation
Immunological diagnosis of Hypocomplementemic Urticarial Vasculitis (detection of C1q antibodies)
AZM - Academisch Ziekenhuis Maastricht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

NETHERLANDS

Limburg
MAASTRICHT

Accreditation
Immunological diagnosis of Goodpasture Syndrome (detection of GBM antibodies)
AZM - Academisch Ziekenhuis Maastricht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of hereditary immune deficiencies (Panel)
Hôpital Necker-Enfants Malades
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

ITALY

LAZIO
ROMA

Molecular diagnosis of suceptibility to Behçet disease (HLA-B gene)
Azienda Ospedaliera S. Camillo-Forlanini - Ospedale San Camillo
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

CAMPANIA
NAPOLI

Diagnosis of susceptibility to Behcet's disease (HLA-B gene)
Biotecnologie Avanzate Srl
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

FRANCE

NOUVELLE AQUITAINE
BORDEAUX

Diagnosis of susceptibility to Behcet disease (lymphotoxicity and HLA-B51 genotyping)
CHU de Bordeaux-GH Pellegrin
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics, Immunology
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

PORTUGAL

CENTRO
OEIRAS

Analysis of susceptibility for Behcet disease (HLA-B gene, 51 allele)
Laboratório de Análises Clínicas Dr. Joaquim Chaves
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

PORTUGAL

ILHAS
FUNCHAL

Molecular diagnosis of Behcet disease (HLA-B gene, 51 allele: Sequencing of the exon 2 and 3)
Universidade da Madeira
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of susceptibility to Behçet disease (HLA-B gene: PCR-SSO)
CHU Paris-GH St-Louis Lariboisière F.Widal - Hôpital Saint-Louis
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

GRAND-EST
REIMS

Diagnosis of predisposition to Behçet disease (HLA-B*51:01 gene)
CHU de Reims - Hôpital Robert Debré
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

SPAIN

Comunidad Valenciana
ELCHE

Diagnosis of autoinflamatory syndrome and related disorders (gene panel)
Bioarray
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

AUSTRIA

WIEN
WIEN

Molecular diagnosis of vasculitis due to ADA2 deficiency (ADA2 gene)
Medizinische Universität Wien
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

SPAIN

Madrid
MADRID

Diagnosis of autoinflammatory diseases (panel)
Hospital Universitario Fundación Jiménez Díaz
Purpose(s) : Antenatal diagnosis, Pre-implantation diagnosis, Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

SPAIN

Madrid
MADRID

Diagnosis of inflammatory and autoimmune disease with epilepsy (panel)
Hospital Universitario Fundación Jiménez Díaz
Purpose(s) : Antenatal diagnosis, Pre-implantation diagnosis, Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

SPAIN

Cataluña
BARCELONA

Diagnosis of vasculitis due to ADA2 deficiency (ADA2 gene)
Hospital Universitari Vall d'Hebron
Purpose(s) : Pre-implantation diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

Diagnosis of neurotransmitter defects and related diseases (panel)
Hospital Sant Joan de Déu Barcelona
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

Diagnosis of Rett syndrome and epilepsy (panel)
Hospital Sant Joan de Déu Barcelona
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

Diagnosis of vasculopathy (panel)
Hospital Sant Joan de Déu Barcelona
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

Diagnosis of inherited cancer-predisposing syndrome (panel)
Hospital Sant Joan de Déu Barcelona
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

SPAIN

Madrid
TRES CANTOS

Diagnosis of vasculitis due to ADA2 deficiency (ADA2 gene)
Centro de estudios genéticos ATG Medical
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

Diagnosis of immunodeficiency (panel)
Hospital Sant Joan de Déu Barcelona
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

Diagnosis of congenital deafness (panel)
Hospital Sant Joan de Déu Barcelona
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

ITALY

EMILIA ROMAGNA
FERRARA

Diagnosis of Behçet disease (HLA-B gene)
A.O.U. di Ferrara - Polo Chimico-Bio-Medico
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

CENTRE-VAL DE LOIRE
TOURS

Diagnosis of predisposition to Behçet disease (HLA-B gene)
Établissement Français du Sang - Centre Atlantique
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

AUSTRIA

WIEN
WIEN

Diagnosis of Vasculitis due to ADA2 deficiency (ADA2 gene)
Hanusch Krankenhaus
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES), Sanger sequencing

SPAIN

Galicia
A CORUÑA

Diagnosis of rare genetic immune disease (panel - 458 genes)
Health In Code
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

SPAIN

Galicia
A CORUÑA

Diagnosis of primary immunodeficiency (panel - 301 genes)
Health In Code
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

SPAIN

Galicia
A CORUÑA

Diagnosis of glomerular disease (panel - 52 genes)
Health In Code
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

SPAIN

Galicia
A CORUÑA

Diagnosis of Behçet disease (panel - 27 genes)
Health In Code
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of Wegener granulomatosis (search for anti-cytoplasm antibodies of neutrophilic polynuclears ANCA)
Hôpital Necker-Enfants Malades
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of microscopic polyangiitis (search of anti-cytoplasm antibodies of neutrophilic polynuclears ANCA)
Hôpital Necker-Enfants Malades
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Immunological diagnosis of giant cell arteritis
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Immunological diagnosis of Behçet disease
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Immunological diagnosis of Churg-Strauss syndrome
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Immunological diagnosis of Cogan syndrome
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Immunological diagnosis of cryoglobulinemia
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Immunological diagnosis of Wegener granulomatosis
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Immunological diagnosis of juvenile temporal arteritis
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Immunological diagnosis of polyarteritis nodosa
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Immunological diagnosis of rheumatoid purpura
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Immunological diagnosis of Takayasu arteritis
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

AUSTRIA

OBERÖSTERREICH
LINZ

Immunological diagnosis of Goodpasture syndrome (anti-GBM antibodies in serum)
TRULAB - Medizinisches Chemisches Laboratorium
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

AUSTRIA

OBERÖSTERREICH
LINZ

Immunological diagnosis of ANCA-associated vasculitis (total ANCA, anti-PR3, anti-MPO)
TRULAB - Medizinisches Chemisches Laboratorium
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

AUSTRIA

STEIERMARK
GRAZ

Immunological diagnosis of Goodpasture syndrome (anti-GBM antibodies in serum)
Medizinische Universität Graz
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

GERMANY

Niedersachsen
HANNOVER

Diagnosis of cryoglobulinemia
Medizinische Hochschule Hannover
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

GERMANY

Niedersachsen
HANNOVER

Diagnosis of Wegener granulomatosis
Medizinische Hochschule Hannover
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

GERMANY

Niedersachsen
HANNOVER

Diagnosis of microscopic polyangiitis (ANCA)
Medizinische Hochschule Hannover
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

FRANCE

AUVERGNE-RHONE-ALPES
GRENOBLE

Diagnosis of complement deficiency acquired during hypocomplementaemic leucocytoclasic vasculitis : anti-C1q antibodies
CHU de Grenoble et des Alpes - Institut de biologie et de pathologie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

FRANCE

ILE-DE-FRANCE
LE KREMLIN-BICÊTRE

Diagnosis of vasculitis on nerve and muscle biospy
CHU Paris-Sud - Hôpital de Bicêtre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Pathology

ITALY

EMILIA ROMAGNA
REGGIO EMILIA

Molecular diagnosis of Behçet disease
IRCCS Arcispedale Santa Maria Nuova
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
KIRCHHEIM UNTER TECK

Diagnosis of vasculitides (ANCA, ANA, ACPA, cryoglobulins, lymphocyte phenotyping, BAL)
medius Klinik Kirchheim
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

PUGLIA
BARI

Immunological diagnosis of cryoglobulinemia
Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

MOLISE
POZZILLI

Molecular diagnosis of susceptibility to Behcet's disease (HLA-B 51 gene)
Istituto Neurologico Mediterraneo - IRCCS Neuromed
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

AUSTRIA

WIEN
WIEN

Immunological diagnosis of ANCA-associated vasculitis (total ANCA, anti-PR3, anti-MPO)
Medizinische Universität Wien
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

AUSTRIA

WIEN
WIEN

Immunological diagnosis of Goodpasture syndrome (anti-GBM antibodies in serum)
Medizinische Universität Wien
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

AUSTRIA

STEIERMARK
GRAZ

Immunological diagnosis of ANCA-associated vasculitis (total ANCA, anti-PR3, anti-MPO)
Medizinische Universität Graz
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

FRANCE

AUVERGNE-RHONE-ALPES
CLERMONT-FERRAND

Diagnosis of susceptibility to Behcet disease (HLA-B gene)
CHU de Clermont-Ferrand - Hôpital Gabriel Montpied
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques