SE-ATLAS

15q13.3 microdeletion syndrome 1p36 deletion syndrome ARX-related epileptic encephalopathy Acute disseminated encephalomyelitis Adult-onset myasthenia gravis Aicardi syndrome Arnold-Chiari malformation type I Arnold-Chiari malformation type II Bazex-Dupré-Christol syndrome Behçet disease Birt-Hogg-Dubé syndrome Brooke-Spiegler syndrome Colorado tick fever Congenital rubella syndrome Congenital smooth muscle hamartoma Congenital toxoplasmosis Cutaneous neuroendocrine carcinoma Cystic fibrosis Dermatofibrosarcoma protuberans Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome Eastern equine encephalitis Encephalitis lethargica Enthesitis-related juvenile idiopathic arthritis Extramammary Paget disease Familial atypical multiple mole melanoma syndrome Familial keratoacanthoma Familial melanoma Familial multiple fibrofolliculoma Familial syringomyelia Familial tumoral calcinosis Fetal cytomegalovirus syndrome Full NF2-related schwannomatosis Gardner syndrome Generalized basaloid follicular hamartoma syndrome Generalized eruptive keratoacanthoma Gorlin syndrome Granulomatosis with polyangiitis Granulomatous slack skin Hemihyperplasia-multiple lipomatosis syndrome Hemimegalencephaly Hereditary leiomyomatosis and renal cell cancer Hereditary neurocutaneous malformation Herpes simplex virus encephalitis Holoprosencephaly Hypothalamic hamartomas with gelastic seizures Idiopathic syringomyelia Incontinentia pigmenti Infantile myofibromatosis Ito hypomelanosis Juvenile idiopathic arthritis Juvenile myasthenia gravis KCNQ2-related epileptic encephalopathy KDM5C-related syndromic X-linked intellectual disability Kleefstra syndrome due to 9q34 microdeletion Klüver-Bucy syndrome La Crosse encephalitis Lethal neonatal spasticity-epileptic encephalopathy syndrome Limbic encephalitis Lissencephaly Malignant melanoma of the mucosa Meningococcal meningitis Microlissencephaly-micromelia syndrome Miller-Dieker syndrome Morvan syndrome Muir-Torre syndrome Multiple self-healing squamous epithelioma Myasthenia gravis Mycoplasma encephalitis Neuroectodermal melanolysosomal disease Neurofibromatosis type 1 Non-syndromic cerebral malformation due to abnormal neuronal migration Oculocerebrocutaneous syndrome Oligoarticular juvenile idiopathic arthritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Overlapping connective tissue disease PEHO syndrome PEHO-like syndrome PTEN hamartoma tumor syndrome Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome Pediatric systemic lupus erythematosus Pilomatrixoma Pneumococcal meningitis Polyarticular juvenile idiopathic arthritis Polymicrogyria with optic nerve hypoplasia Porencephaly Primary cutaneous lymphoma Primary syringomyelia Progressive hemifacial atrophy Proliferating trichilemmal cyst Proteus syndrome Psoriasis-related juvenile idiopathic arthritis Rare nail tumor Rare nevus Rare skin tumor or hamartoma Rare systemic or rheumatological disease of childhood Rasmussen subacute encephalitis Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Ring chromosome 14 syndrome Ring chromosome 20 syndrome Rombo syndrome Rubella panencephalitis Sarcoidosis Schizencephaly Secondary syringomyelia Severe neonatal-onset encephalopathy with microcephaly St. Louis encephalitis Subacute sclerosing leukoencephalitis Subcutaneous panniculitis-like T-cell lymphoma Superficial fibromatosis Syringocystadenoma papilliferum Syringomyelia Systemic-onset juvenile idiopathic arthritis Tetrasomy 12p Thiamine-responsive encephalopathy Tick-borne encephalitis Transient neonatal myasthenia gravis Trichofolliculoma Tuberous sclerosis complex Unexplained long-lasting fever/inflammatory syndrome Unspecified juvenile idiopathic arthritis W syndrome West-Nile encephalitis Western equine encephalitis Wilson disease Wolf-Hirschhorn syndrome