SE-ATLAS

4H leukodystrophy Adrenomyeloneuropathy Adult Krabbe disease Adult-onset autosomal dominant leukodystrophy Aicardi-Goutières syndrome Alagille syndrome Alagille syndrome due to 20p12 microdeletion Alagille syndrome due to a JAG1 point mutation Alagille syndrome due to a NOTCH2 point mutation Alexander disease Alexander disease type I Alexander disease type II Allan-Herndon-Dudley syndrome Alpha-1-antitrypsin deficiency Anti-neutrophil cytoplasmic antibody-associated vasculitis Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Autoinflammatory syndrome of childhood Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Behçet disease Blau syndrome CACH syndrome CADDS CANDLE syndrome CINCA syndrome CLN1 disease CLN10 disease CLN2 disease CLN5 disease CLN6 disease CLN7 disease CLN8 disease CLN9 disease CREST syndrome Canavan disease Cerebrotendinous xanthomatosis Cogan syndrome Congenital neuronal ceroid lipofuscinosis Congenital or early infantile CACH syndrome Cree leukoencephalopathy Cryoglobulinemic vasculitis Cystic leukoencephalopathy without megalencephaly DITRA Drug-induced vasculitis Early-onset sarcoidosis Enthesitis-related juvenile idiopathic arthritis Eosinophilic fasciitis Eosinophilic granulomatosis with polyangiitis Fabry disease Familial Mediterranean fever Familial cold urticaria Genetic glomerular disease Giant cell arteritis Gorham-Stout disease Granulomatosis with polyangiitis Granulomatous autoinflammatory syndrome of childhood Hajdu-Cheney syndrome Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia Hereditary periodic fever syndrome Hyperimmunoglobulinemia D with periodic fever Hypocomplementemic urticarial vasculitis Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome Hypomyelination with atrophy of basal ganglia and cerebellum Hypomyelination with brain stem and spinal cord involvement and leg spasticity Hypomyelination-congenital cataract syndrome Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome Idiopathic juvenile osteoporosis Idiopathic recurrent pericarditis Immunoglobulin A vasculitis Infantile Krabbe disease Infantile Refsum disease Infantile neuronal ceroid lipofuscinosis Infantile onset panniculitis with uveitis and systemic granulomatosis JMP syndrome Juvenile dermatomyositis Juvenile idiopathic arthritis Juvenile neuronal ceroid lipofuscinosis Juvenile or adult CACH syndrome Juvenile polymyositis Kawasaki disease Krabbe disease Late infantile CACH syndrome Late infantile neuronal ceroid lipofuscinosis Late-infantile/juvenile Krabbe disease Leukodystrophy Leukoencephalopathy with bilateral anterior temporal lobe cysts Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome Leukoencephalopathy with mild cerebellar ataxia and white matter edema Leukoencephalopathy-dystonia-motor neuropathy syndrome Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Localized scleroderma Majeed syndrome Megalencephalic leukoencephalopathy with subcortical cysts Metachromatic leukodystrophy Metachromatic leukodystrophy, adult form Metachromatic leukodystrophy, juvenile form Metachromatic leukodystrophy, late infantile form Microscopic polyangiitis Mild Canavan disease Mixed autoinflammatory and autoimmune syndrome Mixed connective tissue disease Mixed cryoglobulinemia type II Mixed cryoglobulinemia type III Muckle-Wells syndrome NLRP12-associated hereditary periodic fever syndrome NLRP3-associated autoinflammatory disease Nakajo-Nishimura syndrome Nasu-Hakola disease Neonatal adrenoleukodystrophy Non-infectious anterior uveitis Null syndrome OBSOLETE: CLN3 disease Odontoleukodystrophy Oligoarticular juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Ovarioleukodystrophy Overlapping connective tissue disease PAPA syndrome PFAPA syndrome PLCG2-associated antibody deficiency and immune dysregulation Pediatric Castleman disease Pediatric systemic lupus erythematosus Pelizaeus-Merzbacher disease Pelizaeus-Merzbacher disease in female carriers Pelizaeus-Merzbacher disease, classic form Pelizaeus-Merzbacher disease, connatal form Pelizaeus-Merzbacher disease, transitional form Pelizaeus-Merzbacher-like disease Pelizaeus-Merzbacher-like disease due to AIMP1 mutation Pelizaeus-Merzbacher-like disease due to GJC2 mutation Pelizaeus-Merzbacher-like disease due to HSPD1 mutation Periodic fever syndrome of childhood Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease Peroxisomal acyl-CoA oxidase deficiency Peroxisome biogenesis disorder Polyarticular juvenile idiopathic arthritis Postinfectious vasculitis Primary Sjögren syndrome Primary glomerular disease Progressive cavitating leukoencephalopathy Proteasome-associated autoinflammatory syndrome Psoriasis-related juvenile idiopathic arthritis Pyogenic autoinflammatory syndrome of childhood Rare pediatric systemic disease Rare pediatric vasculitis Rare systemic or rheumatological disease of childhood Ravine syndrome Reactive arthritis Refsum disease Relapsing polychondritis Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis STXBP1-related encephalopathy Sarcoidosis Secondary glomerular disease Severe Canavan disease Spastic paraplegia type 2 Sterile multifocal osteomyelitis with periostitis and pustulosis Sweet syndrome Systemic-onset juvenile idiopathic arthritis Takayasu arteritis Thrombotic microangiopathy Tumor necrosis factor receptor 1 associated periodic syndrome Unclassified autoinflammatory syndrome of childhood Unclassified vasculitis Unexplained long-lasting fever/inflammatory syndrome Unexplained periodic fever syndrome of childhood Unknown leukodystrophy Unspecified juvenile idiopathic arthritis Vasculitis due to ADA2 deficiency Wilson disease X-linked adrenoleukodystrophy X-linked cerebral adrenoleukodystrophy Zellweger syndrome