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 Juvenile idiopathic arthritis Full NF2-related schwannomatosis Hemihyperplasia-multiple lipomatosis syndrome Hemimegalencephaly Unexplained long-lasting fever/inflammatory syndrome Granulomatous slack skin Gorlin syndrome 1p36 deletion syndrome PEHO-like syndrome Hereditary neurocutaneous malformation PEHO syndrome Rombo syndrome Bazex-Dupré-Christol syndrome Familial tumoral calcinosis Brooke-Spiegler syndrome Sarcoidosis Holoprosencephaly Schizencephaly Behçet disease Western equine encephalitis Miller-Dieker syndrome Birt-Hogg-Dubé syndrome Colorado tick fever Progressive hemifacial atrophy Tuberous sclerosis complex Eastern equine encephalitis Acute disseminated encephalomyelitis Pediatric systemic lupus erythematosus Kleefstra syndrome due to 9q34 microdeletion Superficial fibromatosis Encephalitis lethargica Rare nevus 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 Generalized eruptive keratoacanthoma Dermatofibrosarcoma protuberans Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Congenital rubella syndrome Familial atypical multiple mole melanoma syndrome Secondary syringomyelia Primary syringomyelia Rasmussen subacute encephalitis Idiopathic syringomyelia Fetal cytomegalovirus syndrome Klüver-Bucy syndrome Herpes simplex virus encephalitis 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 Limbic encephalitis Wilson disease