SE-ATLAS

Adrenomyeloneuropathy Adult Krabbe disease Aicardi-Goutières syndrome Alexander disease Alexander disease type I Alexander disease type II Allan-Herndon-Dudley syndrome Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Autoimmune interstitial lung disease-arthritis syndrome Autosomal dominant polycystic kidney disease Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers CACH syndrome CADDS CREST syndrome Canavan disease Cerebrotendinous xanthomatosis Cervical spina bifida aperta Cervical spina bifida cystica Chronic intestinal failure Congenital diaphragmatic hernia Congenital or early infantile CACH syndrome Cree leukoencephalopathy Cystic leukoencephalopathy without megalencephaly Diaphragmatic or abdominal wall malformation Diffuse cutaneous systemic sclerosis Enthesitis-related juvenile idiopathic arthritis Eosinophilic fasciitis Gastroschisis Hemophilia A Hemophilia B Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia 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 Infantile Krabbe disease Infantile Refsum disease Juvenile dermatomyositis Juvenile idiopathic arthritis Juvenile or adult CACH syndrome Juvenile polymyositis Kawasaki disease Krabbe disease Late infantile CACH syndrome Late-infantile/juvenile Krabbe disease 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 Lumbosacral spina bifida aperta Lumbosacral spina bifida cystica Megalencephalic leukoencephalopathy with subcortical cysts Mild Canavan disease Mild hemophilia A Mild hemophilia B Mixed connective tissue disease Moderate hemophilia A Moderate hemophilia B Nasu-Hakola disease Neonatal antiphospholipid syndrome Neonatal autoimmune hemolytic anemia Neonatal dermatomyositis Neonatal lupus erythematosus Neonatal scleroderma Null syndrome Odontoleukodystrophy Oligoarticular juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Omphalocele Open spinal dysraphism Ovarioleukodystrophy Overlapping connective tissue disease 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 Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease Peroxisome biogenesis disorder Polyarticular juvenile idiopathic arthritis Progressive cavitating leukoencephalopathy Psoriasis-related juvenile idiopathic arthritis Rare gastroenterologic disease Rare intestinal disease Rare pediatric systemic disease Ravine syndrome Refsum disease 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 STAT3-related early-onset multisystem autoimmune disease Sarcoidosis Secondary neonatal autoimmune disease Severe Canavan disease Severe hemophilia A Severe hemophilia B Spastic paraplegia type 2 Spina bifida and other spinal dysraphisms Spina bifida-hypospadias syndrome Spinal dysraphism with a posterior meningocele Systemic sclerosis Systemic-onset juvenile idiopathic arthritis Total spina bifida aperta Total spina bifida cystica Transient neonatal myasthenia gravis Unexplained long-lasting fever/inflammatory syndrome Unspecified juvenile idiopathic arthritis Von Willebrand disease Von Willebrand disease type 1 Von Willebrand disease type 2 Von Willebrand disease type 3 Zellweger syndrome