SE-ATLAS

Thrombotic microangiopathy Kawasaki disease Infantile neuronal ceroid lipofuscinosis Pelizaeus-Merzbacher disease Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Alagille syndrome due to a JAG1 point mutation OBSOLETE: CLN3 disease Cryoglobulinemic vasculitis Unspecified juvenile idiopathic arthritis PLCG2-associated antibody deficiency and immune dysregulation Oligoarticular juvenile idiopathic arthritis CLN2 disease CLN5 disease CLN9 disease Nasu-Hakola disease Neonatal adrenoleukodystrophy Relapsing polychondritis Autosomal dominant polycystic kidney disease Metachromatic leukodystrophy, late infantile form Enthesitis-related juvenile idiopathic arthritis Allan-Herndon-Dudley syndrome Metachromatic leukodystrophy, juvenile form Infantile onset panniculitis with uveitis and systemic granulomatosis 4H leukodystrophy Metachromatic leukodystrophy, adult form Familial Mediterranean fever Hyperimmunoglobulinemia D with periodic fever Idiopathic recurrent pericarditis Sterile multifocal osteomyelitis with periostitis and pustulosis Overlapping connective tissue disease Pelizaeus-Merzbacher disease in female carriers Unknown leukodystrophy 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 Infantile Refsum disease Zellweger syndrome Unclassified vasculitis Odontoleukodystrophy Metachromatic leukodystrophy Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia JMP syndrome Hypomyelination-hypogonadotropic hypogonadism-hypodontia 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 Alagille syndrome due to 20p12 microdeletion Canavan disease Juvenile polymyositis NLRP3-associated autoinflammatory disease 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 Nakajo-Nishimura syndrome Alexander disease Granulomatous autoinflammatory syndrome of childhood 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 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 Cogan syndrome Tumor necrosis factor receptor 1 associated periodic syndrome Unexplained long-lasting fever/inflammatory syndrome Takayasu arteritis Blau syndrome CLN10 disease Alagille syndrome due to a NOTCH2 point mutation STXBP1-related encephalopathy CINCA syndrome Majeed syndrome Primary Sjögren syndrome Non-infectious anterior uveitis Early-onset sarcoidosis PAPA-Syndrom Ceroid-Lipofuszinose, neuronale, spät-infantile Seltene systemische Krankheit des Kindes Alpha-1-Antitrypsin-Mangel Autoinflammatorisches Syndrom, pyogenes, der Kindheit Vaskulitis durch ADA2-Mangel Riesenzell-Arteriitis Megalenzephale Leukoenzephalopathie mit subkortikalen Zysten CREST-Syndrom Leukoenzephalopathie mit beiderseitigen vorderen Temporallappen-Zysten Kälte-Urtikaria, familiäre Osteoporose, idiopathische juvenile Immunoglobulin A-Vaskulitis Epilepsie, progressive - Intelligenzminderung, Finnischer Typ Ceroid-Lipofuszinose, neuronale Seltene systemische oder rheumatologische Krankheit der Kindheit Dermatomyositis, juvenile Refsum-Krankheit Ovarioleukodystrophie Ravine-Syndrom CACH-Syndrom, juvenile oder adulte Form Glomerulopathie, genetisch bedingte Seltene Vaskulitis des Kindes NLRP12-assoziiertes hereditäres Periodisches Fiebersyndrom DITRA Peroxisomenbiogenesedefekt Fasziitis, eosinophile Adrenoleukodystrophie, X-chromosomale, zerebrale Form CANDLE-Syndrom PFAPA-Syndrom Pelizaeus-Merzbacher-Krankheit, klassische Form Leukoenzephalopathie-Ataxie-Hypodontie-Hypomyelinisierung-Syndrom Hypomyelinisierung - kongenitale Katarakt Null-Syndrom Sklerodermie, zirkumskripte Arthritis, idiopathische juvenile polyartikuläre, Rheumafaktor-positive Hajdu-Cheney-Syndrom Pelizaeus-Merzbacher-ähnliche Krankheit mit HSPD1-Genmutationen Castleman-Krankheit des Kindesalters Vaskulitis mit assoziierten antineutrophilen zytoplasmatischen Antikörpern CLN8-Krankheit Leukodystrophie CLN6-Krankheit Juvenile neuronale Ceroid-Lipofuszinose, ATP13A2-assoziierte Cree-Leukoenzephalopathie CACH-Syndrom, kongenitales oder früh-infantile Form Ceroid-Lipofuszinose, neuronale, kongenitale Alagille-Syndrom Arthritis, idiopathische juvenile, Rheumafaktor-negative, ohne anti-nukleäre Antikörper Hereditäres periodisches Fiebersyndrom Muckle-Wells-Syndrom Autoinflammatorisches und autoimmunes Syndrom, gemischtes Gorham-Stout-Krankheit Periodisches Fiebersyndrom der Kindheit Lupus erythematodes, systemischer, des Kindesalters Adrenomyeloneuropathie CACH-Syndrom Acyl-CoA-Oxidase-Mangel, peroxisomaler Ceroid-Lipofuszinose, neuronale, adulte Hypomyelinisierung mit Atrophie der Basalganglien und des Kleinhirns Arthritis, idiopathische juvenile, Psoriasis-assoziierte Vaskulitis, Medikamenten-induzierte Alexander-Krankheit Typ I Spastische Paraplegie Typ 2 Alexander-Krankheit Typ II Leukodystrophie, autosomal-dominante, im Erwachsenenalter beginnend Polyangiitis, mikroskopische Nierenkrankheit, polyzystische, autosomal-rezessive Pelizaeus-Merzbacher-ähnliche Krankheit mit AIMP1-Genmutationen Autoinflammatorisches Syndrom der Kindheit Krabbe-Syndrom CLN1-Krankheit