SE-ATLAS

Mikroangiopathie, thrombotische Kawasaki-Krankheit Ceroid-Lipofuszinose, neuronale, infantile Pelizaeus-Merzbacher-Krankheit Arthritis, idiopathische juvenile, oligoartikuläre, ohne anti-nukleäre Antikörper Alagille-Syndrom durch JAG1-Gen-Punktmutationen Kryoglobulinämische Vaskulitis Arthritis, idiopathische juvenile, unklassifizierte PLCG2-associated antibody deficiency and immune dysregulation Arthritis, idiopathische juvenile, oligoartikuläre CLN2-Krankheit CLN5-Krankheit CLN9-Krankheit Nasu-Hakola-Krankheit Adrenoleukodystrophie, neonatale Form Polychondritis, rezidivierende Nierenkrankheit, polyzystische, autosomal-dominante Leukodystrophie, metachromatische, spät-infantile Form 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 Perikarditis, idiopathische rekurrente Sterile multifokale Osteomyelitis mit Periostitis und Pustulose Mischkollagenose, überlappende Pelizaeus-Merzbacher-Krankheit, weibliche Überträgerinnen Leukodystrophie unbekannter Ursache Glomerulopathie, primäre Krabbe-Syndrom, infantile Form Unerklärliches periodisches Fierbersyndrom der Kindheit Pelizaeus-Merzbacher-Krankheit, transitionale Form Krabbe-Syndrom, spät-infantiles oder juveniles Granulomatose mit Polyangiitis Leukoenzephalopathie-Thalamus und Hirnstamm-Anomalien-Hoher Laktatwert-Syndrom Krabbe-Syndrom, mit Beginn im Erwachsenenalter Refsum-Krankheit, infantile Form Zellweger-Syndrom Vaskulitis, unklassifizierte Odontoleukodystrophie Leukodystrophie, metachromatische Hereditäre diffuse Leukoenzephalopathie mit axonalen Sphäroiden und pigmentierter Glia JMP-Syndrom Hypomyelinisierung-Hypogonadotroper Hypogonadismus-Hypodontie-Syndrom Glomerulopathie, sekundäre Pelizaeus-Merzbacher-ähnliche Krankheit Mischkollagenose Pelizaeus-Merzbacher-ähnliche Krankheit mit GJC2-Genmutationen Vaskulitis, hypokomplementämische urtikarielle Canavan-Krankheit, milde Alagille-Syndrom durch Mikrodeletion 20p12 Canavan-Krankheit Polymyositis, juvenile Cryopyrin-assoziiertes periodisches Syndrom CLN7-Krankheit Leukoenzephalopathie mit milder zerebellärer Ataxie und Ödem der weißen Substanz 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 syndrome 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 Immunoglobulin A vasculitis Progressive epilepsy-intellectual disability syndrome, Finnish type Neuronal ceroid lipofuscinosis Rare systemic or rheumatological disease of childhood Juvenile dermatomyositis Refsum disease Ovarioleukodystrophy Ravine syndrome Juvenile or adult CACH syndrome Genetic glomerular disease Rare pediatric vasculitis NLRP12-associated hereditary periodic fever syndrome DITRA Peroxisome biogenesis disorder Eosinophilic fasciitis X-linked cerebral adrenoleukodystrophy CANDLE syndrome PFAPA syndrome Pelizaeus-Merzbacher disease, classic form Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome Hypomyelination-congenital cataract syndrome Null syndrome Localized scleroderma Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Hajdu-Cheney syndrome Pelizaeus-Merzbacher-like disease due to HSPD1 mutation Pediatric Castleman disease Anti-neutrophil cytoplasmic antibody-associated vasculitis CLN8 disease Leukodystrophy CLN6 disease ATP13A2-related juvenile neuronal ceroid lipofuscinosis Cree leukoencephalopathy Congenital or early infantile CACH syndrome Congenital neuronal ceroid lipofuscinosis Alagille syndrome Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies Hereditary periodic fever syndrome Muckle-Wells syndrome Mixed autoinflammatory and autoimmune syndrome Gorham-Stout disease Periodic fever syndrome of childhood Pediatric systemic lupus erythematosus Adrenomyeloneuropathy CACH syndrome Peroxisomal acyl-CoA oxidase deficiency Adult neuronal ceroid lipofuscinosis Hypomyelination with atrophy of basal ganglia and cerebellum Psoriasis-related juvenile idiopathic arthritis Drug-induced vasculitis Alexander disease type I Spastic paraplegia type 2 Alexander disease type II Adult-onset autosomal dominant leukodystrophy Microscopic polyangiitis Autosomal recessive polycystic kidney disease Pelizaeus-Merzbacher-like disease due to AIMP1 mutation Autoinflammatory syndrome of childhood Krabbe disease CLN1 disease