SE-ATLAS

Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Incontinentia pigmenti Extramammary Paget disease W syndrome Subacute sclerosing leukoencephalitis Proliferating trichilemmal cyst Full NF2-related schwannomatosis Behçet disease Birt-Hogg-Dubé syndrome Rare nevus Syringomyelia Polymicrogyria with optic nerve hypoplasia Malignant melanoma of the mucosa Familial atypical multiple mole melanoma syndrome Rasmussen subacute encephalitis Fetal cytomegalovirus syndrome Hypothalamic hamartomas with gelastic seizures KCNQ2-related epileptic encephalopathy Hereditary neurocutaneous malformation Gorlin syndrome Generalized eruptive keratoacanthoma Wilson disease Colorado tick fever Herpes simplex virus encephalitis Unspecified juvenile idiopathic arthritis Morvan syndrome Congenital smooth muscle hamartoma Secondary syringomyelia Primary syringomyelia Rare systemic or rheumatological disease of childhood Miller-Dieker syndrome Idiopathic syringomyelia PEHO syndrome West-Nile encephalitis Pilomatrixoma Wolf-Hirschhorn syndrome La Crosse encephalitis Rare skin tumor or hamartoma Mycoplasma encephalitis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Sarcoidosis St. Louis encephalitis Primary cutaneous lymphoma KDM5C-related syndromic X-linked intellectual disability Schizencephaly Infantile myofibromatosis Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome Congenital rubella syndrome Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Cutaneous neuroendocrine carcinoma Rombo syndrome Tick-borne encephalitis Gardner syndrome Aicardi syndrome Limbic encephalitis Hemihyperplasia-multiple lipomatosis syndrome Hemophilia B 1p36 deletion syndrome PTEN hamartoma tumor syndrome Cystic fibrosis Familial syringomyelia Microlissencephaly-micromelia syndrome Porencephaly Lethal neonatal spasticity-epileptic encephalopathy syndrome Brooke-Spiegler syndrome Western equine encephalitis Non-syndromic cerebral malformation due to abnormal neuronal migration Acute disseminated encephalomyelitis Kleefstra syndrome due to 9q34 microdeletion Ring chromosome 14 syndrome Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Ring chromosome 20 syndrome Systemic-onset juvenile idiopathic arthritis Ito hypomelanosis Thiamine-responsive encephalopathy Generalized basaloid follicular hamartoma syndrome Progressive hemifacial atrophy Meningococcal meningitis Familial tumoral calcinosis Multiple self-healing squamous epithelioma Hemimegalencephaly Rare nail tumor ARX-related epileptic encephalopathy Hemophilia A Syringocystadenoma papilliferum Muir-Torre syndrome Familial multiple fibrofolliculoma Arnold-Chiari malformation type I Lissencephaly Granulomatous slack skin Superficial fibromatosis Congenital toxoplasmosis Juvenile idiopathic arthritis Trichofolliculoma Polyarticular juvenile idiopathic arthritis Subcutaneous panniculitis-like T-cell lymphoma Pneumococcal meningitis Familial melanoma Oculocerebrocutaneous syndrome Arnold-Chiari malformation type II Bazex-Dupré-Christol syndrome Pediatric systemic lupus erythematosus Holoprosencephaly Tetrasomy 12p Neurofibromatosis type 1 Klüver-Bucy syndrome Granulomatosis with polyangiitis Dermatofibrosarcoma protuberans Eastern equine encephalitis Encephalitis lethargica 15q13.3 microdeletion syndrome Rubella panencephalitis Oligoarticular juvenile idiopathic arthritis Neuroectodermal melanolysosomal disease Overlapping connective tissue disease Psoriasis-related juvenile idiopathic arthritis Enthesitis-related juvenile idiopathic arthritis Unexplained long-lasting fever/inflammatory syndrome Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome Severe neonatal-onset encephalopathy with microcephaly PEHO-like syndrome Proteus syndrome Familial keratoacanthoma