SE-ATLAS

Mikroangiopathie, thrombotische CLN1-Krankheit Kawasaki-Krankheit Pelizaeus-Merzbacher-ähnliche Krankheit mit AIMP1-Genmutationen Cree-Leukoenzephalopathie Ovarioleukodystrophie Leukoenzephalopathie-Ataxie-Hypodontie-Hypomyelinisierung-Syndrom Ceroid-Lipofuszinose, neuronale, infantile Pelizaeus-Merzbacher-Krankheit Arthritis, idiopathische juvenile, oligoartikuläre, ohne anti-nukleäre Antikörper Autoinflammatorisches Syndrom der Kindheit Alagille-Syndrom durch JAG1-Gen-Punktmutationen OBSOLET: CLN3-Krankheit Kryoglobulinämische Vaskulitis Fasziitis, eosinophile Arthritis, idiopathische juvenile, unklassifizierte Muckle-Wells-Syndrom PLCG2-associated antibody deficiency and immune dysregulation Arthritis, idiopathische juvenile, oligoartikuläre CLN2-Krankheit Hereditäres periodisches Fiebersyndrom CLN5-Krankheit Arthritis, idiopathische juvenile, Rheumafaktor-negative, ohne anti-nukleäre Antikörper CLN9-Krankheit Nasu-Hakola-Krankheit CACH-Syndrom, kongenitales oder früh-infantile Form CLN6-Krankheit Ceroid-Lipofuszinose, neuronale, kongenitale Adrenoleukodystrophie, neonatale Form Autoinflammatorisches und autoimmunes Syndrom, gemischtes Polyangiitis, mikroskopische Polychondritis, rezidivierende Hypomyelinisierung mit Atrophie der Basalganglien und des Kleinhirns Nierenkrankheit, polyzystische, autosomal-dominante Nierenkrankheit, polyzystische, autosomal-rezessive Periodisches Fiebersyndrom der Kindheit Fabry-Syndrom Alagille-Syndrom CACH-Syndrom, juvenile oder adulte Form Leukodystrophie, metachromatische, spät-infantile Form Seltene systemische oder rheumatologische Krankheit der Kindheit Hypomyelinisierung - kongenitale Katarakt Arthritis, idiopathische juvenile, Psoriasis-assoziierte Arthritis, idiopathische juvenile, Enthesitis-assoziierte Allan-Herndon-Dudley-Syndrom Leukodystrophie, metachromatische, juvenile Form Pannikulitis mit Uveitis und systemischer Granulomatose, infantile Form 4H-Leukodystrophie Leukodystrophie, metachromatische, adulte Form Mittelmeerfieber, familiäres Hyperimmunglobulinämie D mit Rückfallfieber Gorham-Stout-Krankheit Perikarditis, idiopathische rekurrente Pelizaeus-Merzbacher-Krankheit, klassische Form Sterile multifokale Osteomyelitis mit Periostitis und Pustulose Mischkollagenose, überlappende Pelizaeus-Merzbacher-Krankheit, weibliche Überträgerinnen Krabbe-Syndrom Leukodystrophie unbekannter Ursache Primary glomerular disease Infantile Krabbe disease Unexplained periodic fever syndrome of childhood Pelizaeus-Merzbacher disease, transitional form Late-infantile/juvenile Krabbe disease Granulomatosis with polyangiitis Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Adult Krabbe disease Drug-induced vasculitis Infantile Refsum disease Null syndrome Zellweger syndrome Alexander disease type I Unclassified vasculitis Odontoleukodystrophy Metachromatic leukodystrophy Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia Juvenile dermatomyositis Peroxisomal acyl-CoA oxidase deficiency JMP syndrome Pediatric Castleman disease Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome Pediatric systemic lupus erythematosus CANDLE syndrome Secondary glomerular disease Pelizaeus-Merzbacher-like disease Mixed connective tissue disease Pelizaeus-Merzbacher-like disease due to GJC2 mutation Hypocomplementemic urticarial vasculitis Mild Canavan disease Spastic paraplegia type 2 CACH syndrome Pelizaeus-Merzbacher-like disease due to HSPD1 mutation Hajdu-Cheney syndrome Alagille syndrome due to 20p12 microdeletion Canavan disease Juvenile polymyositis Adrenomyeloneuropathy Adult-onset autosomal dominant leukodystrophy Leukodystrophy NLRP3-associated autoinflammatory disease Ravine syndrome CLN7 disease Leukoencephalopathy with mild cerebellar ataxia and white matter edema CADDS Late infantile CACH syndrome Reactive arthritis Severe Canavan disease Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Sarcoidosis X-linked adrenoleukodystrophy Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Postinfectious vasculitis Aicardi-Goutières syndrome Rare pediatric vasculitis Nakajo-Nishimura syndrome Alexander disease NLRP12-associated hereditary periodic fever syndrome Granulomatous autoinflammatory syndrome of childhood Peroxisome biogenesis disorder Juvenile idiopathic arthritis Unclassified autoinflammatory syndrome of childhood Polyarticular juvenile idiopathic arthritis Leukoencephalopathy-dystonia-motor neuropathy syndrome Mixed cryoglobulinemia type III Mixed cryoglobulinemia type II Proteasome-associated autoinflammatory syndrome Behçet disease Wilson disease Cerebrotendinous xanthomatosis Cystic leukoencephalopathy without megalencephaly Hypomyelination with brain stem and spinal cord involvement and leg spasticity PFAPA syndrome Pelizaeus-Merzbacher disease, connatal form Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease Juvenile neuronal ceroid lipofuscinosis Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Systemic-onset juvenile idiopathic arthritis Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome Sweet syndrome Progressive cavitating leukoencephalopathy Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Eosinophilic granulomatosis with polyangiitis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Cogan syndrome Tumor necrosis factor receptor 1 associated periodic syndrome Unexplained long-lasting fever/inflammatory syndrome Alexander disease type II Takayasu arteritis Blau syndrome CLN10 disease Alagille syndrome due to a NOTCH2 point mutation Refsum disease STXBP1-related encephalopathy X-linked cerebral adrenoleukodystrophy CINCA syndrome Majeed syndrome DITRA Primary Sjögren syndrome Localized scleroderma Non-infectious anterior uveitis Early-onset sarcoidosis CLN8 disease PAPA syndrome Genetic glomerular disease Late infantile neuronal ceroid lipofuscinosis Rare pediatric systemic disease Alpha-1-antitrypsin deficiency Pyogenic autoinflammatory syndrome of childhood Vasculitis due to ADA2 deficiency Giant cell arteritis Megalencephalic leukoencephalopathy with subcortical cysts CREST syndrome Leukoencephalopathy with bilateral anterior temporal lobe cysts Familial cold urticaria Idiopathic juvenile osteoporosis Anti-neutrophil cytoplasmic antibody-associated vasculitis Immunoglobulin A vasculitis