SE-ATLAS

Lissenzephalie Arnold-Chiari-Fehlbildung Typ I Seltene systemische oder rheumatologische Krankheit der Kindheit Arthritis, idiopathische juvenile polyartikuläre, Rheumafaktor-positive Arthritis, idiopathische juvenile, Psoriasis-assoziierte Arthritis, idiopathische juvenile, Enthesitis-assoziierte Syndrom der generalisierten basaloiden follikulären Hamartome Incontinentia pigmenti Meningokokkenmeningitis Hamartom der glatten Muskulatur, kongenitales Proteus-Syndrom Fibrofollikulom, familiäres multiples Tetrasomie 12p Letale neonatale Spastik-epileptische Enzephalopathie-Syndrom Mikrolissenzephalie-Mikromelie-Syndrom Paget-Syndrom, extramammär Melanom, familiäres Porenzephalie Ringchromosom-14-Syndrom W-Syndrom Leukoenzephalitis, sklerosierende subakute Enzephalopathie, Thiamin-responsive Mischkollagenose, überlappende Ringchromosom-20-Syndrom Granulomatose mit Polyangiitis Trichilemmalzyste, proliferierende Zerebrale Fehlbildung durch neuronalen Migrationsdefekt, nichtsyndromal Keratoakanthom, familiäres Neurofibromatose Typ 1 Full NF2-related schwannomatosis Juvenile idiopathic arthritis Hemihyperplasia-multiple lipomatosis syndrome Hemimegalencephaly Unexplained long-lasting fever/inflammatory syndrome Granulomatous slack skin 1p36 deletion syndrome PEHO-like syndrome PEHO syndrome Rombo syndrome Bazex-Dupré-Christol syndrome Familial tumoral calcinosis Brooke-Spiegler syndrome Sarcoidosis Holoprosencephaly Behçet disease Schizencephaly Western equine encephalitis Miller-Dieker syndrome Birt-Hogg-Dubé syndrome Progressive hemifacial atrophy Eastern equine encephalitis Acute disseminated encephalomyelitis Pediatric systemic lupus erythematosus Kleefstra syndrome due to 9q34 microdeletion Superficial fibromatosis Rare nevus Encephalitis lethargica Morvan syndrome Primary cutaneous lymphoma ARX-related epileptic encephalopathy Infantile myofibromatosis Familial syringomyelia Subcutaneous panniculitis-like T-cell lymphoma Rare skin tumor or hamartoma West-Nile encephalitis Pneumococcal meningitis Syringomyelia Rubella panencephalitis Wolf-Hirschhorn syndrome Multiple self-healing squamous epithelioma Mycoplasma encephalitis Polymicrogyria with optic nerve hypoplasia Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome Oculocerebrocutaneous syndrome Gardner syndrome St. Louis encephalitis Severe neonatal-onset encephalopathy with microcephaly La Crosse encephalitis Malignant melanoma of the mucosa Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Familial atypical multiple mole melanoma syndrome Congenital rubella syndrome Primary syringomyelia Rasmussen subacute encephalitis Idiopathic syringomyelia Klüver-Bucy syndrome Fetal cytomegalovirus syndrome Syringocystadenoma papilliferum Hypothalamic hamartomas with gelastic seizures Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Tick-borne encephalitis Ito hypomelanosis Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis Neuroectodermal melanolysosomal disease Pilomatrixoma PTEN hamartoma tumor syndrome Unspecified juvenile idiopathic arthritis Systemic-onset juvenile idiopathic arthritis Cutaneous neuroendocrine carcinoma KDM5C-related syndromic X-linked intellectual disability Congenital toxoplasmosis Cystic fibrosis KCNQ2-related epileptic encephalopathy Muir-Torre syndrome Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome Malformation d'Arnold-Chiari type II Trichofolliculome Arthrite juvénile idiopathique polyarticulaire Syndrome de microdélétion 15q13.3 Tumeur rare des ongles Syndrome d'Aicardi Syringomyélie secondaire Malformation neurocutanée héréditaire Encéphalite limbique Myasthénie auto-immune Syndrome de Gorlin Kératoacanthome éruptif généralisé Dermatofibrosarcome de Darier-Ferrand Maladie de Wilson Fièvre à tiques du Colorado Encéphalite à herpes simplex