SE-ATLAS

Lissencephaly Arnold-Chiari malformation type I Rare systemic or rheumatological disease of childhood Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Psoriasis-related juvenile idiopathic arthritis Enthesitis-related juvenile idiopathic arthritis Generalized basaloid follicular hamartoma syndrome Incontinentia pigmenti Meningococcal meningitis Congenital smooth muscle hamartoma Proteus syndrome Familial multiple fibrofolliculoma Tetrasomy 12p Lethal neonatal spasticity-epileptic encephalopathy syndrome Microlissencephaly-micromelia syndrome Melanom, familiäres Paget-Syndrom, extramammär Porenzephalie Ringchromosom-14-Syndrom W-Syndrom Leukoenzephalitis, sklerosierende subakute Enzephalopathie, Thiamin-responsive Mischkollagenose, überlappende Ringchromosom-20-Syndrom Granulomatose mit Polyangiitis Zerebrale Fehlbildung durch neuronalen Migrationsdefekt, nichtsyndromal Trichilemmalzyste, proliferierende Keratoakanthom, familiäres Neurofibromatose Typ 1 Schwannomatose, NF2-assoziierte Arthritis, idiopathische juvenile Hemihyperplasie-multiples Lipomatosis-Syndrom Hemimegalenzephalie Fieber-Syndrom, langanhaltendes unerklärbares Haut, granulomatöse schlaffe 1p36-Deletionssyndrom PEHO-ähnliches Syndrom PEHO-Syndrom Rombo-Syndrom Bazex-Dupré-Christol-Syndrom Tumorale Kalzinose, familiäre Brooke-Spiegler-Syndrom Sarkoidose Holoprosenzephalie Behçet-Syndrom Schizenzephalie Westliche Pferdeenzephalitis Miller-Dieker-Syndrom Birt-Hogg-Dubé-Syndrom Hemiatrophia facialis progressiva Östliche Pferdeenzephalitis Enzephalomyelitis, akute disseminierte Lupus erythematodes, systemischer, des Kindesalters Kleefstra-Syndrom durch Mikrodeletion 9q34 Fibromatose, superfizielle Seltener Naevus Encephalitis lethargica Morvan-Syndrom Lymphom, kutanes primäres Enzephalopathie, epileptische, ARX-assoziierte Myofibromatose, infantile Syringomyelie, familiäre T-Zell-Lymphom, subkutanes Pannikulitis-ähnliches Hauttumor oder Hamartom, seltene Formen West-Nil-Enzephalitis Syringomyelie Pneumokokken-Meningitis Röteln-Panenzephalitis Wolf-Hirschhorn-Syndrom Multiple selbstheilende squamöse Epitheliome Polymikrogyrie mit Sehnerv-Hypoplasie Mykoplasmen-Enzephalitis 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 Malignant melanoma of the mucosa La Crosse encephalitis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Familial atypical multiple mole melanoma syndrome Congenital rubella syndrome Rasmussen subacute encephalitis Primary syringomyelia Idiopathic syringomyelia Klüver-Bucy syndrome Fetal cytomegalovirus syndrome Syringocystadenoma papilliferum Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Hypothalamic hamartomas with gelastic seizures 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 Arnold-Chiari malformation type II Trichofolliculoma Polyarticular juvenile idiopathic arthritis 15q13.3 microdeletion syndrome Rare nail tumor Aicardi syndrome Hereditary neurocutaneous malformation Limbic encephalitis Generalized eruptive keratoacanthoma Colorado tick fever Gorlin syndrome Dermatofibrosarcoma protuberans Wilson disease Herpes simplex virus encephalitis Secondary syringomyelia