SE-ATLAS

Microangiopathie thrombotique Maladie CLN1 Maladie de Kawasaki Maladie de Pelizaeus-Merzbacher-like par mutation de AIMP1 Leucoencéphalopathie crie Ovarioleucodystrophie Syndrome de leucoencéphalopathie-ataxie-hypodontie-hypomyélinisation Céroïde-lipofuscinose neuronale infantile Maladie de Pelizaeus-Merzbacher Arthrite juvénile idiopathique oligoarticulaire sans anticorps anti-noyaux Syndrome auto-inflammatoire de l'enfant Syndrome d'Alagille dû à une mutation ponctuelle de JAG1 OBSOLETE : Maladie CLN3 Vascularite cryoglobulinémique Fasciite à éosinophiles Arthrite juvénile idiopathique indéterminée Syndrome de Muckle-Wells Dérèglement et déficit immunitaire lié à PLCG2 Arthrite juvénile idiopathique oligoarticulaire Maladie CLN2 Syndrome de fièvre récurrente héréditaire Maladie CLN5 Arthrite juvénile idiopathique sans facteur rhumatoïde sans anticorps anti-nucléaire Maladie CLN9 Maladie de Nasu-Hakola Syndrome CACH congénital ou infantile à début précoce Maladie CLN6 Céroïde-lipofuscinose neuronale congénitale Adrénoleucodystrophie néonatale Syndrome mixte auto-inflammatoire et auto-immun Polyangéite microscopique Polychondrite atrophiante Hypomyélinisation avec atrophie des noyaux gris centraux et du cervelet Polykystose rénale autosomique dominante Polykystose rénale autosomique récessive Syndrome de fièvre récurrente de l'enfant Maladie de Fabry Syndrome d'Alagille Syndrome CACH juvénile ou de l'adulte Leucodystrophie métachromatique infantile tardive Maladie systémique ou rhumatologique rare de l'enfant Syndrome d'hypomyélinisation-cataracte congénitale Arthrite juvénile idiopathique associée au psoriasis Arthrite juvénile idiopathique associée aux enthésopathies Syndrome d'Allan-Herndon-Dudley Leucodystrophie métachromatique juvénile Panniculite infantile avec uvéite et granulomatose systémique Leucodystrophie 4H Leucodystrophie métachromatique de l'adulte Fièvre méditerranéenne familiale Syndrome de fièvre périodique avec hyperimmunoglobulinémie D Maladie de Gorham-Stout Péricardite récurrente idiopathique Maladie de Pelizaeus-Merzbacher, forme classique Ostéomyélite stérile multifocale avec périostéite et pustulose Maladie de chevauchement du tissu conjonctif Pelizaeus-Merzbacher disease in female carriers Krabbe disease 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 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