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 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 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 Juvenile dermatomyositis Juvenile or adult CACH syndrome 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 Moderate hemophilia A Moderate hemophilia B Nasu-Hakola disease Neonatal antiphospholipid syndrome Neonatal autoimmune hemolytic anemia Neonatal dermatomyositis Neonatal scleroderma Null syndrome Odontoleukodystrophy Omphalocele Open spinal dysraphism Ovarioleukodystrophy Pediatric Castleman disease 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 Progressive cavitating leukoencephalopathy Ravine syndrome 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 Total spina bifida aperta Total spina bifida cystica Transient neonatal myasthenia gravis Von Willebrand disease Von Willebrand disease type 1 Von Willebrand disease type 2 Von Willebrand disease type 3 Zellweger syndrome