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 Karzinom, kutanes neuroendokrines Rombo-Syndrom Zeckenenzephalitis Gardner-Syndrom Aicardi-Syndrom Limbische Enzephalitis Hemihyperplasie-multiples Lipomatosis-Syndrom Hämophilie B 1p36-Deletionssyndrom PTEN-Hamartom-Tumor-Syndrom Zystische Fibrose Syringomyelie, familiäre Mikrolissenzephalie-Mikromelie-Syndrom Porenzephalie Letale neonatale Spastik-epileptische Enzephalopathie-Syndrom Brooke-Spiegler-Syndrom Westliche Pferdeenzephalitis Zerebrale Fehlbildung durch neuronalen Migrationsdefekt, nichtsyndromal Enzephalomyelitis, akute disseminierte Kleefstra-Syndrom durch Mikrodeletion 9q34 Ringchromosom-14-Syndrom Arthritis, idiopathische juvenile polyartikuläre, Rheumafaktor-negative Ringchromosom-20-Syndrom Arthritis, idiopathische juvenile, systemische Hypomelanose Typ Ito Enzephalopathie, Thiamin-responsive Syndrom der generalisierten basaloiden follikulären Hamartome Hemiatrophia facialis progressiva Meningokokkenmeningitis Tumorale Kalzinose, familiäre Multiple selbstheilende squamöse Epitheliome Hemimegalenzephalie Nageltumor, seltener ARX-related epileptic encephalopathy Hémophilie A Syringocystadénome papillifère Syndrome de Muir-Torre Fibrofolliculomes multiples familiaux Malformation d'Arnold-Chiari type I Lissencéphalie Chalazodermie granulomateuse Fibromatose superficielle Toxoplasmose congénitale Arthrite juvénile idiopathique Trichofolliculome Arthrite juvénile idiopathique polyarticulaire T-Zell-Lymphom, subkutanes Pannikulitis-ähnliches Pneumokokken-Meningitis Melanom, familiäres Okulo-zerebro-kutanes Syndrom Arnold-Chiari-Fehlbildung Typ II Bazex-Dupré-Christol-Syndrom Lupus erythematodes, systemischer, des Kindesalters Holoprosenzephalie Tetrasomie 12p Neurofibromatose Typ 1 Klüver-Bucy-Syndrom Granulomatose mit Polyangiitis Dermatofibrosarcoma protuberans Östliche Pferdeenzephalitis Encephalitis lethargica Mikrodeletionssyndrom 15q13.3 Röteln-Panenzephalitis Arthritis, idiopathische juvenile, oligoartikuläre Neuroektodermale melanolysosomale Krankheit Mischkollagenose, überlappende 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