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 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 Maladie de Refsum Ovarioleucodystrophie Syndrome Ravine Syndrome CACH juvénile ou de l'adulte Néphropathie glomérulaire génétique Vascularite rare de l'enfant Syndrome de fièvre périodique héréditaire lié à NLRP12 DITRA Anomalie de la biogenèse du péroxysome Fasciite à éosinophiles Adrénoleucodystrophie liée à l'X, forme cérébrale Syndrome CANDLE Syndrome PFAPA Maladie de Pelizaeus-Merzbacher, forme classique Syndrome de leucoencéphalopathie-ataxie-hypodontie-hypomyélinisation Syndrome d'hypomyélinisation-cataracte congénitale Maladie de Pelizaeus-Merzbacher par mutation non-sens de PLP1 Sclérodermie localisée Arthrite juvénile idiopathique polyarticulaire avec facteur rhumatoïde Syndrome de Hajdu-Cheney Maladie de Pelizaeus-Merzbacher-like par mutation de HSPD1 Maladie de Castleman de l'enfant Vascularite associée aux anticorps antineutrophiles cytoplasmiques aladie CLN8 Leucodystrophie Maladie CLN6 Céroïde-lipofuscinose neuronale juvénile associée à ATP13A2 Leucoencéphalopathie crie Syndrome CACH congénital ou infantile à début précoce Céroïde-lipofuscinose neuronale congénitale Syndrome d'Alagille Arthrite juvénile idiopathique sans facteur rhumatoïde sans anticorps anti-nucléaire Syndrome de fièvre récurrente héréditaire Syndrome de Muckle-Wells Syndrome mixte auto-inflammatoire et auto-immun Maladie de Gorham-Stout Syndrome de fièvre récurrente de l'enfant Lupus érythémateux disséminé de l'enfant Adrénomyéloneuropathie Syndrome CACH Déficit en acyl-CoA oxydase Céroïde-lipofuscinose neuronale de l'adulte Hypomyélinisation avec atrophie des noyaux gris centraux et du cervelet Arthrite juvénile idiopathique associée au psoriasis Vascularite induite par les médicaments Maladie d'Alexander type I Paraplégie spastique type 2 Maladie d'Alexander type II Leucodystrophie autosomique dominante de l'adulte Polyangéite microscopique Polykystose rénale autosomique récessive Maladie de Pelizaeus-Merzbacher-like par mutation de AIMP1 Syndrome auto-inflammatoire de l'enfant Maladie de Krabbe Maladie CLN1