SE-ATLAS

CLN1 disease Thrombotic microangiopathy Kawasaki disease Pelizaeus-Merzbacher-like disease due to AIMP1 mutation Cree leukoencephalopathy Ovarioleukodystrophy Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome Infantile neuronal ceroid lipofuscinosis Pelizaeus-Merzbacher disease Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Autoinflammatory syndrome of childhood Alagille syndrome due to a JAG1 point mutation OBSOLETE: CLN3 disease Cryoglobulinemic vasculitis Eosinophilic fasciitis Muckle-Wells syndrome PLCG2-associated antibody deficiency and immune dysregulation Unspecified juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis CLN2 disease Hereditary periodic fever syndrome CLN5 disease Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies CLN9 disease Nasu-Hakola disease Congenital or early infantile CACH syndrome CLN6 disease Congenital neuronal ceroid lipofuscinosis Neonatal adrenoleukodystrophy Mixed autoinflammatory and autoimmune syndrome Microscopic polyangiitis Relapsing polychondritis Hypomyelination with atrophy of basal ganglia and cerebellum Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Periodic fever syndrome of childhood Fabry disease Alagille syndrome Juvenile or adult CACH syndrome Metachromatic leukodystrophy, late infantile form Rare systemic or rheumatological disease of childhood Hypomyelination-congenital cataract syndrome Psoriasis-related juvenile idiopathic arthritis 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 Gorham-Stout disease Sterile multifocal osteomyelitis with periostitis and pustulosis Pelizaeus-Merzbacher disease, classic form Overlapping connective tissue disease Pelizaeus-Merzbacher disease in female carriers Krabbe disease Primary glomerular disease Unknown leukodystrophy Infantile Krabbe disease Pelizaeus-Merzbacher disease, transitional form Unexplained periodic fever syndrome of childhood 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 Unclassified vasculitis Alexander disease type I 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 Alagille syndrome due to 20p12 microdeletion Hajdu-Cheney syndrome Canavan disease Adrenomyeloneuropathy Juvenile polymyositis Adult-onset autosomal dominant leukodystrophy NLRP3-associated autoinflammatory disease Ravine syndrome CLN7 disease Leukoencephalopathy with mild cerebellar ataxia and white matter edema CADDS Late infantile CACH syndrome Arthritis, reaktive Canavan-Krankheit, schwere Arthritis, idiopathische juvenile, oligoartikuläre, mit anti-nukleären Antikörpern Sarkoidose Adrenoleukodystrophie, X-chromosomale Arthritis, idiopathische juvenile, Rheumafaktor-negative, mit anti-nukleären Antikörpern Vaskulitis, postinfektiöse Aicardi-Goutières-Syndrom Seltene Vaskulitis des Kindes Nakajo-Nishimura-Syndrom Alexander-Krankheit Leukodystrophie Autoinflammatorisches Syndrom, granulomatöses, der Kindheit Peroxisomenbiogenesedefekt Arthritis, idiopathische juvenile Autoinflammatorisches Syndrom, unklassifiziertes, der Kindheit Arthritis, idiopathische juvenile, polyartikuläre Leukoenzephalopathie - Dystonie - motorische Neuropathie Kryoglobulinämie, gemischte, Typ III Kryoglobulinämie, gemischte, Typ II Proteasom-assoziiertes autoinflammatorisches Syndrom Behçet-Syndrom Wilson-Krankheit Xanthomatose, zerebrotendinöse Zystische Leukoenzephalopathie ohne Megalenzephalie Hypomyelinisierung mit Hirnstamm- und Rückenmarkbeteiligung und Beinspastik PFAPA-Syndrom Pelizaeus-Merzbacher-Krankheit, konnatale Form Periphere demyelinisierende Neuropathie-zentrale demyelinisierende Leukodystrophie-Waardenburg-Syndrom-Hirschsprung Krankheit Ceroid-Lipofuszinose, neuronale, juvenile Arthritis, idiopathische juvenile polyartikuläre, Rheumafaktor-negative Arthritis, idiopathische juvenile, systemische Leukoenzephalopathie mit Hirnstamm- und Rückenmarkbeteiligung - Laktaterhöhung Sweet-Syndrom Leukoenzephalopathie, kavitierende progressive Autoinflammation mit PLCG2-assoziiertem Antikörper-Mangel und Immundysregulation Eosinophile Granulomatose mit Polyangiitis Arthritis, idiopathische juvenile polyartikuläre, Rheumafaktor-positive Cogan-Syndrom Tumornekrosefaktor-Rezeptor 1-assoziiertes periodisches Fieber-Syndrom Fieber-Syndrom, langanhaltendes unerklärbares Alexander-Krankheit Typ II Takayasu-Arteriitis Blau-Syndrom CLN10-Krankheit Alagille-Syndrom durch NOTCH2-Gen-Punktmutationen NLRP12-assoziiertes hereditäres Periodisches Fiebersyndrom STXBP1-abhängige Enzephalopathie Adrenoleukodystrophie, X-chromosomale, zerebrale Form CINCA-Syndrom Majeed-Syndrom Refsum-Krankheit Sjögren-Syndrom, primäres Sklerodermie, zirkumskripte Uveitis, anteriore, nicht-infektiöse Form Sarkoidose, früh beginnende DITRA CLN8-Krankheit PAPA-Syndrom Glomerulopathie, genetisch bedingte 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 Vaskulitis mit assoziierten antineutrophilen zytoplasmatischen Antikörpern Immunoglobulin A-Vaskulitis Juvenile neuronale Ceroid-Lipofuszinose, ATP13A2-assoziierte Epilepsie, progressive - Intelligenzminderung, Finnischer Typ Ceroid-Lipofuszinose, neuronale, adulte Ceroid-Lipofuszinose, neuronale