Sandhoff Disease Smith Lemli Opitz Syndrome Syndrome, Fraser Syndrome, CHARGE Syndrome, Alstrom Stargardt Disease Schnyder crystalline corneal dystrophy Shwachman syndrome Septo-Optic Dysplasia Short chain Acyl CoA dehydrogenase deficiency Systemic carnitine deficiency Sitosterolemia Scleroatonic muscular dystrophy Syndrome, Costello Smith-Magenis Syndrome Simpson-Golabi-Behmel syndrome Schimke immunoosseous dysplasia Sarcoma Spastic paraplegia 2, X-linked Spinocerebellar ataxia 28 Stargardt disease 1 Spinal muscular atrophy with respiratory distress 1 Spastic paraplegia 4, autosomal dominant Syndactyly, type 2 Spondyloepiphyseal dysplasia, congenita SeSAME syndrome Stickler syndrome, type 2 Spastic paraplegia 11, autosomal recessive Spinocerebellar ataxia 27 Spastic paraplegia 15, autosomal recessive Stress-induced polymorphic ventricular tachycardia Schneckenbecken dysplasia Spastic Paraplegia 30, Autosomal Recessive Spastic Paraplegia 7, Autosomal Recessive Spastic Paraplegia 31, Autosomal Dominant Spastic paraplegia 13, autosomal dominant Short QT Syndrome 1 Spondyloepimetaphyseal Dysplasia, Pakistani Type Siderius X-linked mental retardation syndrome Severe combined immunodeficiency with sensitivity to ionizing radiation Spherocytosis, Type 1 Schizophrenias Syndrome, Wolfram Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive Stargardt disease 3 Spinal Muscular Atrophy, Distal, X-Linked 3 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy Spinocerebellar Ataxia 17 Spherocytosis, Type 4 Spinocerebellar Ataxia, Autosomal Recessive 9 Spondylocarpotarsal synostosis Smith-McCort Dysplasia Sjogren-Larsson Syndrome Sturge Weber Syndrome Seckel syndrome 1 Syndrome, Donohue succinic semialdehyde dehydrogenase deficiency Severe combined immunodeficiency due to adenosine deaminase deficiency Spastic paraplegia 20, autosomal recessive Syndrome, Barth Snyder Robinson syndrome SHORT syndrome Squamous cell carcinoma of the head and neck Schwannomatosis Spastic ataxia Charlevoix-Saguenay type Spinocerebellar ataxia, autosomal recessive 1 Spinocerebellar ataxia 14 Stormorken Syndrome Stickler syndrome, type 1 Spherocytosis, Type 3 Spastic paraplegia 17 Syndrome, Waardenburg's Sucrase-isomaltase deficiency, congenital Stuve-Wiedemann syndrome Syndactyly Cenani Lenz type Snowflake vitreoretinal degeneration Schinzel-Giedion syndrome Schindler Disease, Type I Spinocerebellar ataxia 13 Schopf-Schulz-Passarge Syndrome Spondylometaphyseal dysplasia, Kozlowski type Sialic Acid Storage Disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Spastic paraplegia 10, autosomal dominant Spinocerebellar Ataxia 29 Steatocystoma Multiplex Schizencephaly Short rib-polydactyly syndrome, Verma-Naumoff type Spondyloperipheral dysplasia short ulna Split-Hand-Foot Malformation 4 Stapes Ankylosis With Broad Thumb And Toes Spastic paraplegia 3, autosomal dominant Sulfocysteinuria Syndrome, Kallmann's Sclerosteosis Splenic Hypoplasia Syndrome, Bardet-Biedl Shprintzen Golberg craniosynostosis Spinocerebellar ataxia 21 Spinocerebellar ataxia 19 Spinocerebellar Ataxia 15 Spinocerebellar ataxia 23 Spastic Paraplegia Type 8 Short QT Syndrome 3 Spastic Paraplegia 39, Autosomal Recessive Sarcosinemia Strudwick syndrome Spastic paraplegia 6, autosomal dominant Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Stiff Skin Syndrome Sveinsson Chorioretinal Atrophy Spondyloepimetaphyseal dysplasia with multiple dislocations Scalp ear nipple syndrome Status Epilepticus Small Cell Lung Carcinoma Sulfite oxidase deficiency Specific Granule Deficiency Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant Single upper central incisor Skin Fragility-Woolly Hair Syndrome Spondylometaphyseal dysplasia, Sedaghatian type Short Stature, Idiopathic, Autosomal Syndactyly, type 3 Stargardt disease 4 Short QT Syndrome 2 Spheroid body myopathy Segawa syndrome, autosomal recessive Spondylo-Megaepiphyseal-Metaphyseal Dysplasia Sialidase deficiency Sneddon Syndrome Spahr type Metaphyseal chondrodysplasia Striatonigral degeneration infantile Spastic Paraplegia, Optic Atrophy, and Neuropathy Stickler Syndrome, Type I, Nonsyndromic Ocular Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction Spinocerebellar Ataxia, Autosomal Recessive 7 Schindler Disease, Type II Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy Sick Sinus Syndrome 1, Autosomal Recessive Short Stature, Idiopathic, X-Linked Spondyloepimetaphyseal Dysplasia, X-Linked Syndactyly, type v Stomatocytosis I Spondyloepimetaphyseal Dysplasia, Missouri Type Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Spastic Paraplegia 42, Autosomal Dominant Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like Scapuloperoneal Myopathy, X-Linked Dominant Spastic Paraplegia 44, Autosomal Recessive Sarcoidoses Seizure Stevens-Johnson Syndrome Sarcoma, Synovial Syndrome, Silver-Russell Syndrome, Sotos Sarcoma, Alveolar Soft Part Succinyl-CoA:3-oxoacid CoA transferase deficiency Sacral agenesis Spondylometaphyseal dysplasia, 'corner fracture' type Sarcoma, Ewings Spinocerebellar Ataxia, X-Linked 1 Spastic paraplegia 9, autosomal dominant Sick Sinus Syndrome 2, Autosomal Dominant Spinocerebellar ataxia 26 Spastic paraplegia 26, autosomal recessive Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Slowed Nerve Conduction Velocity, Autosomal Dominant Stocco dos Santos syndrome Spinocerebellar ataxia, autosomal recessive 4 Senior-Loken syndrome 4 Seckel syndrome 2 Spastic Paraplegia 5a, Autosomal Recessive Spinocerebellar Ataxia, Autosomal Recessive 8 Spastic Paraplegia 33, Autosomal Dominant Spondylocostal Dysostosis 3, Autosomal Recessive Spinal muscular atrophy, Jerash type Split-Hand-Foot Malformation With Sensorineural Hearing Loss Senior-Loken Syndrome 6 Spastic paraplegia 12, autosomal dominant Spinocerebellar Ataxia 12 Spinocerebellar Ataxia, Autosomal Recessive 2 Spondyloepimetaphyseal dysplasia, Genevieve type Scaphocephaly, Maxillary Retrusion, And Mental Retardation Scapuloperoneal Syndrome, Neurogenic, Kaeser Type Spinocerebellar Ataxia 10 Surfactant Metabolism Dysfunction, Pulmonary, 1 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Surfactant Metabolism Dysfunction, Pulmonary, 3 Surfactant Metabolism Dysfunction, Pulmonary, 2 Spherocytosis, Type 5 Skeletal Defects, Genital Hypoplasia, And Mental Retardation Surfactant Metabolism Dysfunction, Pulmonary, 4 Spondyloepimetaphyseal Dysplasia, Aggrecan Type Split-Hand-Foot Malformation 6 Spastic Paraplegia 18, Autosomal Recessive Syndrome, Heterotaxy Spinocerebellar ataxia 8 Scott Syndrome Spinocerebellar Ataxia 11 Simpson-Golabi-Behmel Syndrome, Type 2 Sick Sinus Syndrome Sudden Infant Death with Dysgenesis of the Testes Syndrome Spinocerebellar Ataxia 31 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, Skeletal Abnormalities Spondylometaphyseal dysplasia, axial Spondyloepimetaphyseal Dysplasia With Joint Laxity Spastic Paraplegia 28, Autosomal Recessive Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly Spondyloepiphyseal Dysplasia, Kimberley Type Spinocerebellar ataxia, autosomal recessive 5 Syndactyly, Type IV Spondylometaphyseal dysplasia with dentinogenesis imperfecta Spastic Paraplegia-50, Autosomal Recessive Stomach Ulcer Strokes Syndrome, Williams Sepsis Sclerotylosis Spastic paraplegia 23 Solitary Fibrous Tumors Salivary Gland Adenoma, Pleomorphic Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative Senior-Loken Syndrome 5 Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Spondylocostal dysostosis, autosomal recessive Sacral defect and anterior sacral meningocele Synpolydactyly 2 Spongiform Encephalopathy with Neuropsychiatric Features Seborrhea-Like Dermatitis with Psoriasiform Elements Spinal Muscular Atrophy, Late-Onset, Finkel Type Stickler syndrome, type 3 Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs Spondyloenchondrodysplasia Scrapie Split hand foot deformity 1 Spastic Paraplegia Type 7 Striatal Degeneration, Autosomal Dominant Subcutaneous panniculitis-like T-cell lymphoma Sezary Syndrome Short Rib Polydactyly Syndrome SPINAL MUSCULAR ATROPHIES CHILDHOOD Self-Healing Collodion Baby Spastic paraplegia type 5A, recessive Scleroderma, Systemic Shock, Hemorrhagic Silicoses Spondylitis, Ankylosing Syndactyly Schindler Disease, Type III Saccharopinuria Sjogren's Syndrome Sarcoglycanopathies Spinocerebellar Ataxia with Epilepsy Severe Dengue Scolioses Syncope Spondyloepimetaphyseal Dysplasia, Shohat Type Syndrome, Bartter's Sleep Initiation and Maintenance Disorders Sarcoma, Kaposi Seminoma Skin Ulcer Splenomegaly Stereotypic Movement Disorder Sarcoma, Endometrial Stromal Sarcoma, Clear Cell Sertoli-Leydig Cell Tumor Sex Cord-Gonadal Stromal Tumors Spermatogenesis arrest Solitary Kidney Short rib-polydactyly syndrome, Beemer type Spinal Muscular Atrophy, Type IV Striatonigral Degeneration, Infantile, Mitochondrial Sandhoff Disease, Adult Type Sandhoff Disease, Juvenile Type Saethre-Chotzen Syndrome with Eyelid Anomalies Skin-Hair-Eye Pigmentation, Variation In, 11 Spermatogenic Failure 7 Short Qt Syndrome Schwartz-Lelek syndrome Sex Development Disorder Stomatitides Syndrome, Tumour Lysis Sinusitides Staphylococcal Infections Syndrome, HELLP Salcedo syndrome Small Fibre Neuropathy Seasonal Allergic Rhinitis Stuttering Syndrome, Uveomeningoencephalitic Stiff Person Syndrome Syndrome, Kleine-Levin Sexual precocity Schnitzler Syndrome Severe Acute Respiratory Syndrome Spondyloepimetaphyseal dysplasia, sponastrime type ST Elevation Myocardial Infarction Schizophrenia, Childhood Shock, Septic Sialorrhea Sick Building Syndrome Skin Abnormalities Speech Disorders Spinal Cord Disease Substance Withdrawal Syndrome Synovitides Schmid-Fraccaro syndrome Sarcopenia Spinocerebellar ataxia 25 Spinocerebellar ataxia, autosomal recessive 3 Scalp defect, congenital Sialidoses, type 2 Sarcoma, Experimental Schistosomiases Schistosomiasis mansoni Scleroses Sensation Disorders Sertoli Cell Tumor Serum Sickness Shock Shock, Cardiogenic Shy Drager Syndrome Sneezing Somatoform Disorder Spasm Spina Bifida Cystica Spinal Curvatures Starvation Stress Disorder, Traumatic Superior Vena Cava Syndrome Sinus Tachycardias Supraventricular Tachycardias Sweets Syndrome Stupor Social Communication Disorder Skin Diseases, Vascular Smooth Muscle Tumor Substance-Related Disorders Sexual Dysfunctions, Physiological Stomatognathic System Abnormalities Systemic Vasculitides Sagittal Sinus Thromboses Schizophrenia Spectrum and Other Psychotic Disorders Sacroiliitis Somatosensory Disorder Spinal Epidural Hematoma Sleep Disorders, Circadian Rhythm Spondylarthritides Spondylarthropathies Succinylcholine Sensitivity Sinonasal undifferentiated carcinoma Schilbach-Rott Syndrome Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias Succedaneous Teeth, Agenesis Of Sarcoidosis, Early-Onset Spastic Paraplegia 27, Autosomal Recessive Spinocerebellar ataxia 20 Spermatogenic Failure, Nonobstructive, Y-Linked Spastic Paraplegia 24, Autosomal Recessive Sensorimotor neuropathy with ataxia, autosomal dominant Spastic paraplegia 16, X-linked Spastic paraplegia 19, autosomal dominant Sandhoff Disease, Infantile Type Spondyloocular Syndrome, Autosomal Recessive Spastic paraplegia 14, autosomal recessive Spastic paraplegia 29, autosomal dominant Syndactyly, Type I Split-Hand-Foot Malformation With Long Bone Deficiency 1 Spondyloepimetaphyseal Dysplasia With Abnormal Dentition Spondylometaphyseal dysplasia, Algerian type Sclerocornea, Autosomal Dominant Sacral Agenesis Syndrome Spastic Paraplegia 32, Autosomal Recessive Skin-Hair-Eye Pigmentation, Variation In, 5 Skin-Hair-Eye Pigmentation, Variation In, 4 Spastic Paraplegia 38, Autosomal Dominant Spastic Paraplegia 34, X-Linked Sensorineural Deafness With Mild Renal Dysfunction Spinal muscular atrophy 4 Spinocerebellar ataxia 30 Spastic paraplegia 25, autosomal recessive Spastic Paraplegia 36, Autosomal Dominant Spastic Paraplegia 37, Autosomal Dominant Sebocystomatosis Smad4-Related Juvenile Polyposis Stenosis, Hypertrophic Pyloric Succinate-Coa Ligase Deficiency Spermatic Cord Torsion Salpingitides Sarcoma, Yoshida Scheuermanns Disease Sciatica Shock, Traumatic Sialadenitides Skin Diseases, Genetic Surgical Wound Dehiscence Stenoses, Tracheal Strongylida Infections Subacute Combined Degeneration Systemic Inflammatory Response Syndrome Spinal Cord Vascular Diseases Sertoli Cell-Only Syndrome Spina Bifida, X-Linked Senior-Loken Syndrome 3 Subcortical Band Heterotopia, X-Linked Spina Bifida, Folate-Sensitive Spondylodysplasia And Premature Pubarche Spastic Ataxia Strabismus Sclerocornea Scimitar Syndrome Spondylolistheses Syringomyelia Single Umbilical Artery Scleritides Scotoma Shivering Shyness Signs and Symptoms, Respiratory Smoking Snoring Spermatocele Spondylolyses Steatorrhea Stomach Diverticula Suicides Stenoses, Tricuspid Valve Stricture, Urethral Spina Bifida Occulta Slipped Capital Femoral Epiphyses Sprengel deformity Secretory breast carcinoma Secretory Component Deficiency Suntan Stillbirth Sarcoma family syndrome of Li and Fraumeni Say Meyer syndrome Severe combined immunodeficiency, atypical Spinal Muscular Atrophy, Facioscapulohumeral Type Sella Turcica, Bridged Solitary Pulmonary Nodule Skin-Hair-Eye Pigmentation, Variation In, 9 Skin-Hair-Eye Pigmentation, Variation In, 8 Skin-Hair-Eye Pigmentation, Variation In, 10 Sternal cleft Syndromes, Drug Hypersensitivity Sporadic CJD Sleep Latency Spastic Paraplegia Type 4 Synostoses Salmonella Infections Sarcoidosis, Pulmonary Scrub Typhus Somatostatinoma Sphingolipidoses Superinfection Spinal Tuberculoses Sarcomas, Histiocytic Sideroses Spondylitides Scalded-Skin Syndrome, Staphylococcal Systemic candidiasis Smoldering Multiple Myeloma Stroke, Lacunar Schistosomiasis japonica Smallpox Subungual exostoses Syphilis Sarcomas, Myeloid Syringoma Synkinesis Serpentine fibula polycystic kidney syndrome Split-Hand Foot Malformation 2 Sarcoma 180 Somnambulism Sparganoses Spotted Fever Group Rickettsiosis Struma Ovarii Subacute Thyroiditides Syphilis, secondary Schistosomiasis haematobia Sleep Paralysis Subepithelial Mucinous Corneal Dystrophy Surfactant Dysfunction Speech Sound Disorder Sarcocystoses Scleredema Adultorum Scurvy Sebaceous Gland Diseases Serositides Sexually Transmitted Diseases, Bacterial Spinal Stenoses Spondylosis Sporotrichoses Strongyloidiases Superior Mesenteric Artery Syndrome Swine Vesicular Disease Syphilis, Latent Syndromes, Thoracic Outlet Syncope, Vasovagal Syphilis, tertiary Skin Diseases, Bacterial Skin Diseases, Viral Skin Diseases, Eczematous Syndrome, Aicardi's Splenosis Syndromes, Yellow Nail Synesthesia Stress Disorders, Traumatic, Acute Septal Rupture, Ventricular Syndrome, Chilaiditi's Syndrome, Mirizzi Syndrome, Kluver-Bucy Segmental glomerulosclerosis Solitary Fibrous Tumor, Pleural Sprue, Collagenous Stewart Treves syndrome Spinal Osteochondrosis Stridor, Congenital Sister Mary Joseph's Nodule Squamous Odontogenic Tumor Sulfatidoses Spinocerebellar ataxia, autosomal recessive 6 Spastic Paraplegia, Ataxia, And Mental Retardation Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies Synpolydactyly 3 Storm Syndrome Steinfeld Syndrome Syndrome, Susac Sudden unexpected nocturnal death syndrome Stenotrophomonas maltophilia bacteremia Subacute cerebellar degeneration Syphilis, primary Sclerosing lymphocytic lobulitis Sex Chromosome Disorders of Sex Development Syndrome, May-Thurner Syndromes, Nodding Severe Acute Malnutrition Sacrum Sensation Set (Psychology) Signal Transduction Sleep Somatotype Speech Spermatozoa Spherocyte Spine Stapes Stereotyping Stomach Syndromes Socket, Tooth Sexual Development Short Stature-Obesity Syndrome Spinocerebellar ataxia 22 Split hand foot deformity Sideroblastic anemia, autosomal