SE-ATLAS

Arthritis, idiopathische juvenile polyartikuläre, Rheumafaktor-positive Incontinentia pigmenti Paget-Syndrom, extramammär W-Syndrom Leukoenzephalitis, sklerosierende subakute Trichilemmalzyste, proliferierende Schwannomatose, NF2-assoziierte Behçet-Syndrom Birt-Hogg-Dubé-Syndrom Seltener Naevus Syringomyelie Polymikrogyrie mit Sehnerv-Hypoplasie Malignes Melanom der Mukosa Familiäres atpisches multiples Muttermal- und Melanomsyndrom Rasmussen-Enzephalitis Fetales Zytomegalie-Syndrom Hypothalamus-Hamartom mit gelastischen Anfällen Enzephalopathie, epileptische, KCNQ2-assoziierte Neurokutane Fehlbildung, hereditäre Gorlin-Syndrom Keratoakanthom, eruptives generalisiertes Wilson-Krankheit Colorado-Zeckenfieber Herpes-simplex-Enzephalitis Arthritis, idiopathische juvenile, unklassifizierte Morvan-Syndrom Hamartom der glatten Muskulatur, kongenitales Syringomyelie, sekundäre Syringomyelie, primäre Seltene systemische oder rheumatologische Krankheit der Kindheit Miller-Dieker-Syndrom Syringomyelie, idiopathische PEHO-Syndrom West-Nil-Enzephalitis Pilomatrixom Wolf-Hirschhorn-Syndrom Kalifornische Enzephalitis Hauttumor oder Hamartom, seltene Formen Mykoplasmen-Enzephalitis Arthritis, idiopathische juvenile, oligoartikuläre, mit anti-nukleären Antikörpern Sarkoidose St.-Louis-Enzephalitis Lymphom, kutanes primäres Intelligenzminderung, X-chromosomale, syndromale, Typ Claes-Jensen Schizenzephalie Myofibromatose, infantile Syndrom der partiellen Corpus callosum-Agenesie mit zerebellärer Vermishypoplasie und Zysten der hinteren Schädelgrube 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