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degenerescence book type, Spirochetes disease, Spirurida Infections, Spitz nevus, Spleen neoplasm, Splenic infarcts, Splenogonadal fusion limb defects micrognatia, Splenomegaly, Split hand foot malformation, Split hand foot malformation 1, Split hand split foot malformation autosomal recessive, Split hand split foot mandibular hypoplasia, Split hand split foot nystagmus, Split hand urinary anomalies spina bifida, Split hand/foot malformation X-linked, Spondylarthropathy, Spondylocamptodactyly, Spondylocarpotarsal synostosis syndrome, Spondylocostal dysostosis 1, Spondylocostal dysostosis 2, Spondylocostal dysostosis 3, Spondylocostal dysostosis 4, Spondyloenchondrodysplasia, Spondyloepimetaphyseal dysplasia Genevieve type, Spondyloepimetaphyseal dysplasia joint laxity, Spondyloepimetaphyseal dysplasia Matrilin-3 related, Spondyloepimetaphyseal dysplasia micromelic, Spondyloepimetaphyseal dysplasia Missouri type, Spondyloepimetaphyseal dysplasia Shohat type, Spondyloepimetaphyseal dysplasia Sponastrime type, Spondyloepimetaphyseal dysplasia Strudwick type, Spondyloepimetaphyseal dysplasia with hypotrichosis, Spondyloepimetaphyseal dysplasia with multiple dislocations, Spondyloepimetaphyseal dysplasia X-linked, Spondyloepimetaphyseal dysplasia x-linked with mental deterioration, Spondyloepimetaphyseal dysplasia Aggrecan type, Spondyloepiphyseal dysplasia, Spondyloepiphyseal dysplasia congenita, Spondyloepiphyseal dysplasia Maroteaux type, Spondyloepiphyseal dysplasia Omani type, Spondyloepiphyseal dysplasia tarda autosomal dominant, Spondyloepiphyseal dysplasia tarda progressive arthropathy, Spondyloepiphyseal dysplasia tarda Toledo type, Spondyloepiphyseal dysplasia tarda X-linked, Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech, Spondylohypoplasia arthrogryposis and popliteal pterygium, Spondylometaepiphyseal dysplasia short limb-hand type, Spondylometaphyseal dysplasia Algerian type, Spondylometaphyseal dysplasia axial, Spondylometaphyseal dysplasia corner fracture type, Spondylometaphyseal dysplasia East-African type, Spondylometaphyseal dysplasia Kozlowski type, Spondylometaphyseal dysplasia Sedaghatian type, Spondylometaphyseal dysplasia type A4, Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism, Spondylometaphyseal dysplasia with cone-rod dystrophy, Spondylometaphyseal dysplasia with dentinogenesis imperfecta, Spondylometaphyseal dysplasia X-linked, Spondyloperipheral dysplasia, Spondylospinal thoracic dysostosis, Spondylothoracic dysostosis, Spongiform encephalopathy, Spontaneous coronary artery dissection, Spontaneous periodic hypo<strong>the</strong>rmia, Spontaneous pneumothorax familial type, Sporotrichosis, Spotted fever, Spranger Schinzel Myers syndrome, Sprengel deformity, Squamous cell carcinoma of <strong>the</strong> head and neck, St Anthony's fire, Stachybotrys chartarum, Stalker Chitayat syndrome, Stampe sorensen syndrome, Staphylococcal food poisoning, Staphylococcal toxic shock syndrome, STAR syndrome, Stargardt disease, Stargardt macular degeneration absent or hypoplastic corpus callosum mental retardation and dysmorphic features, Status epilepticus, Steatocystoma multiplex, Steatocystoma multiplex with natal teeth, Steinfeld syndrome, Stenotrophomonas maltophilia, Sterility due to immotile flagella, Stern Lubinsky Durrie syndrome, Page 60/68

Sternal cleft, Sternal cyst vascular anomalies, Sternal malformation vascular dysplasia associatio, Steroid dehydrogenase deficiency dental anomalies, Stevens-Johnson syndrome, Stewart Treves syndrome, Stickler syndrome, Stickler syndrome type 1, Stickler syndrome type 2, Stickler syndrome type 3, Stiff person syndrome, Stiff skin syndrome, Still's disease adult onset, Stocco dos Santos syndrome, Stoelinga de Koomen Davis syndrome, Stoll Alembik Dott syndrome, Stoll alembik finck syndrome, Stoll geraudel chauvin syndrome, Stoll kieny dott syndrome, Stomach cancer childhood, Stomach cancer familial, Stomach carcinoma, Stomatocytosis I, Stomatocytosis II, Storm syndrome, Stratton garcia young syndrome, Stratton Parker syndrome, Streptococcal Group A invasive disease, Streptococcal Group B invasive disease, Stress cardiomyopathy, Striatonigral degeneration infantile, Strongyloidiasis, Stuart factor deficiency congenital, Sturge-Weber syndrome, Stuve-Wiedemann syndrome, Subacute sclerosing panencephalitis, Subaortic stenosis short stature syndrome, Subcutaneous panniculitis-like T-cell lymphoma, Subependymal giant cell astrocytoma, Subependymal nodular heterotopia, Subependymoma, Subpulmonary stenosis, Subvalvular aortic stenosis, Succinic acidemia, Succinic acidemia lactic acidosis congenital, Succinic semialdehyde dehydrogenase deficiency, Succinyl-CoA acetoacetate transferase deficiency, Sudden Arrhythmia Death Syndrome, Sudden infant death syndrome, Sugarman brachydactyly, Sulfite oxidase deficiency, Summitt syndrome, SUNCT headache, Superficial siderosis of <strong>the</strong> central nervous system, Superficial spreading melanoma, Superior mesenteric artery syndrome, Superior vena cava syndrome, Supernumerary nipples, Supraglottic laryngeal cancer, Supranuclear ocular palsy, Supratentorial primitive neuroectodermal tumor, Supratentorial primitive neuroectodermal tumors childhood, Supraumbilical midabdominal raphe and facial cavernous hemangiomas, Susac syndrome, Sutton disease 2, Swyer James syndrome, Swyer syndrome, Sydenham's chorea, Symmastia, Symmetrical thalamic calcifications, Symphalangism brachydactyly, Symphalangism brachydactyly craniosynostosis, Symphalangism distal, Symphalangism familial proximal, Symphalangism short stature accessory testis, Symphalangism with multiple anomalies of hands and feet, Symphalangism distal with microdontia dental pulp stones and narrowed zygomatic arch, Syncamptodactyly scoliosis, Syndactyly cataract mental retardation, Syndactyly Cenani Lenz type, Syndactyly ectodermal dysplasia cleft lip palate hand foot, Syndactyly type 1, Syndactyly type 1 with cataracts and mental retardation, Syndactyly type 2, Syndactyly type 3, Syndactyly type 5, Syndactyly type 9, Syndactyly-polydactyly-earlobe syndrome, Syndesmodysplasic dwarfism, Syngnathia cleft palate, Syngnathia multiple anomalies, Synostoses tarsal carpal and digital, Synostosis of talus and calcaneus short stature, Synovial cancer, Synovial Chondromatosis, Synovial chondromatosis familial with dwarfism, Synovial sarcoma, Synovitis, Synovitis acne pustulosis hyperostosis osteitis, Syphilitic aseptic meningitis, Syphilitic myelopathy, Syringobulbia, Syringocystadenoma papilliferum, Syringomas natal teeth oligodontia, Syringomelia hyperkeratosis, Syringomyelia, Systemic candidiasis, Systemic capillary leak syndrome, Page 61/68