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 Familial melanoma Extramammary Paget disease Porencephaly Ring chromosome 14 syndrome W syndrome Subacute sclerosing leukoencephalitis Thiamine-responsive encephalopathy Overlapping connective tissue disease Ring chromosome 20 syndrome Granulomatosis with polyangiitis Non-syndromic cerebral malformation due to abnormal neuronal migration Proliferating trichilemmal cyst Familial keratoacanthoma Neurofibromatosis type 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 Syringomyelia Pneumococcal meningitis Rubella panencephalitis Wolf-Hirschhorn syndrome Multiple self-healing squamous epithelioma Polymicrogyria with optic nerve hypoplasia Mycoplasma encephalitis 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