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ERN-RITA

ERN-RITA

European Reference Network for Immunodeficiency, Autoinflammatory, Autimmune and Pediatric Rheumatic disea

The European Reference Network that aims at improving the care of patients with Rare Immunological Disorders
  • Reference centers
  • Disease information
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  • Activities
    • MeRITA Registry
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  • Patients
    • ERNs and ePAGs
    • RIPAG
  • About
    • RITA: A Unique Opportunity
    • Mission, Goals and Objectives
    • Governance
    • RITA Membership
    • Scientific societies, stakeholders
    • About ERNS
    • Monitoring
  • Rare diseases
  • Autoimmune diseases (AI)
  • Autoimmune Neuroinflammation Adult and Paediatric
Rare diseases
  • Pediatric Rheumatic diseases (PR)
    • Juvenile Arthritis
    • Miscellaneous
    • Systemic autoimmune disease
    • Bone disease
    • Paediatric vasculitis
  • Autoimmune diseases (AI)
    • Autoimmune systemic vasculitis adult and paediatric
    • Autoimmune Neuroinflammation Adult and Paediatric
  • Autoinflammatory disorders (AID)
    • Defects affecting the inflammasome
    • Non inflammasome-related conditions
    • Type 1 Interferonopathies
    • Monogenic Inflammatory bowel diseases
    • Miscellaneous
  • Primary immunodeficiencies (PID)
    • T−B+ Severe Combined Immunodeficiency (SCID)
    • Isotype or light chain deficiencies with generally normal numbers of B cells
    • Chronic mucocutaneous candidiasis (CMC)
    • T−B− SCID DNA recombination defects
    • Familial hemophagocytic lymphohistiocytosis (FHL) syndromes without hypopigmentation
    • TLR signaling pathway deficiency
    • Combined immunodeficiencies generally less profound than severe combined immunodeficiency
    • Familial hemophagocytic lymphohistiocytosis (FHL) syndromes with hypopigmentation
    • Congenital thrombocytopenia
    • T regulatory cells genetic defects
    • DNA repair defects (other than those in group 1)
    • Autoimmunity with or without lymphoproliferation
    • Thymic defects with additional congenital anomalies
    • Autoimmune lymphoproliferative syndrome (ALPS)
    • Immune-osseous dysplasias
    • Immune dysregulation with colitis
    • Hyper-IgE syndromes (HIES)
    • Type 1 Interferonopathies
    • Dyskeratosis congenita (DKC) with bone marrow failure and dysfunctional telomere maintenance
    • Congenital neutropenias
    • Defects of Vitamin B12 and Folate metabolism
    • Defects of Motility
    • Anhidrotic ectodermaldysplasia with immunodeficiency (EDA-ID)
    • Defects of Respiratory Burst
    • Calcium channel defects
    • Medelian Susceptibility to mycobacterial disease (MSMD)
    • Other defects
    • Epidermodysplasia verruciformis
    • Severe reduction in all serum immunoglobulin isotypes with profoundly decreased or absent B cells
    • Predisposition to severe viral infection
    • Severe reduction in at least 2 serum immunoglobulin isotypes with normal or low number of B cells
    • Herpes simplex encephalitis (HSE)
    • Severe reduction in serum IgG and IgA with normal/elevated IgM and normal numbers of B cells
    • Predisposition to invasive fungal diseases

Autoimmune Neuroinflammation Adult and Paediatric

Disease information Hide
LinksVasculitis - patient informationVasculitis - clinician information
Patient organisations Show
LinksAPACS – Associazione Pazienti Sindrome di Churg-Strauss (EGPA)Vasculitis Finland (SuomenVaskuliittiyhdistys)Vasculitis IrelandVasculitis UKVasculitis Stitching

Diseases

Encephalitis lethargicaDisease detail Limbic encephalitisDisease detail Optic neuritisDisease detail Transverse MyelitisDisease detail SpondyloenchondrodysplasiaDisease detail MarbugDisease detail RhombencephalitisDisease detail Shilder diseaseDisease detail Rassmussen EncephalitisDisease detail Rare central nervous and vascular diseaseDisease detail Primary or secondary lymphohisticytosis affecting CNSDisease detail Inflammatory optic neuritisDisease detail Idiopathic transverse myelitisDisease detail Hashimoto EncephalitisDisease detail Multifocal Motor Neuropathy (MMN)Disease detail Guillain-Barre Syndrome (GBS)Disease detail Neuromyelitis opticaDisease detail Post infectious encephalitisDisease detail Opsoclonus-myoclonus syndromeDisease detail Balo DiseaseDisease detail Autoimmune neuro-inflammatory diseaseDisease detail Autoimmune encephalitisDisease detail Acute demyelinating encephalomyelitisDisease detail
→ Access the newsletter archive

Scientific societies & Patient organisations

Network coordination

UMC Utrecht
Heidelberglaan 100
3584 CX Utrecht
Netherlands
VAT NL004205315B01

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The contents of this webpage are the sole responsibility of ERN-RITA and do not necessarily reflect the opinion of the European Union. 

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