Sacroiliac Joint Dysfunction (Sacroiliac Joint Pain), Safest Rheumatoid Arthritis Drugs During Pregnancy, Salmonella Contagious (Is Salmonella Contagious), Salmonella Food Poisoning (Salmonellosis), Scabies Contagious (Is Scabies Contagious), Scar Tissue (Abdominal Adhesions (Scar Tissue)), Scarlet Fever Contagious (Is Scarlet Fever Contagious), Schizophrenia vs. Bipolar Disorder (Bipolar Disorder vs Schizophrenia), Sciatica: Causes, Exercises, and Symptoms, Sciatica: Causes, Treatment, and Symptoms, Screening For Colon Cancer (Colon Cancer Screening), Screening for Prostate Cancer (Prostate Cancer Screening), Screening Test, Quad Marker (Quad Marker Screen Test), Seborrheic Dermatitis (Seborrheic Dermatitis), Seizure Disorders vs. Seizure (Seizure vs Seizure Disorders Whats the difference), Seizure First Aid (First Aid for Seizures), Seizure Surgery, Children (Pediatric Epilepsy Surgery), Seizure Test (EEG - Electroencephalogram), Seizure vs Seizure Disorders Whats the difference, Self Exam (Breast Cancer Follow-Up Self-Exam), Serious Diseases and Health Problems (Symptoms of Serious Diseases and Health Problems), Serous Cyst Adenomas Pancreas (Pancreatic Cysts), Severe acute respiratory syndrome (Severe Acute Respiratory Syndrome (SARS)), Sex Urinary and Bladder Problems of Diabetes (Sexual and Urologic Problems of Diabetes), Sexual Response Cycle (Phases of Sexual Response), Sexually Transmitted Disease (STD) Treatments, Sexually Transmitted Diseases (STDs In Women), Sexually Transmitted Diseases and Pregnancy (STDs), Shaken Baby Syndrome (Abusive Head Trauma), Shot vs. Salpingitis - refers to inflammation of the fallopian tube. Our experts guide you through symptoms, causes, diagnosis, and treatment options. If you have problems viewing PDF files, download the latest version of Adobe Reader, For language access assistance, contact the NCATS Public Information Officer, Genetic and Rare Diseases Information Center (GARD) - PO Box 8126, Gaithersburg, MD 20898-8126 - Toll-free: 1-888-205-2311, expand submenu for Find Diseases By Category, expand submenu for Patients, Families and Friends, expand submenu for Healthcare Professionals. Linking to a non-federal website does not constitute an endorsement by CDC or any of its employees of the sponsors or the information and … See additional information. Allergies. 2. Digestion. No hemos publicado información en español sobre enfermedades que comiencen con esta letra. Popular Health Centers. Some conditions that are not, Sacral meningocele, conotruncal heart defects, and minor anomalies of head and neck, Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis, Sagittal craniostenosis, bilateral coloboma of the iris, craniofacial dysmorphy, asymmetrical split hand malformation, bilateral syndactyly of 2nd-4th, Sagittal craniosynostosis, Dandy-Walker malformation and hydrocephalus, San Luis Valley recombinant chromosome 8 syndrome, Sarcoma family syndrome of Li and Fraumeni, Sarcoplasmic reticulum -Ca2+ATPase deficiency, Sarcosine dehydrogenase complex deficiency, Say Barber Biesecker Young-Simpson syndrome, SBLA syndrome (Sarcoma, Breast, Leukemia, and Adrenal Gland), SC phocomelia syndrome (mild variant of Roberts syndrome), Scapuloperoneal myopathy, X-linked dominant, Scapuloperoneal syndrome, neurogenic type, of Kaeser, Scapuloperoneal syndrome, X-linked (formerly), Scheie syndrome (subtype) formerly known as Mucopolysaccharidosis type V), Schinzel Giedion midface-retraction syndrome, SCID, AR, T-cell negative, B-cell negative, NK cell-positive, SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, with sensitivity to ionizing radiation, Scleroatrophic and keratotic dermatosis of limbs, Sclerosing dysplasia of bone with ichthyosis and premature ovarian failure, Scoliosis, congenital with unilateral unsegmented bar, Scott craniodigital syndrome with mental retardation, SDHAF2-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome (Paragangliomas 2), SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome, SDHC-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome (Paragangliomas 3), SDHD-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome (Paragangliomas 1), SDHx-related paraganglioma-pheochromocytoma, Seizures - sensorineural deafness - ataxia - intellectual disability - electrolyte imbalance, Seizures, sensorineural deafness, ataxia, mental retardation and electrolyte imbalance, Seizures-sensorineural deafness-ataxia-intellectual disability-electrolyte imbalance syndrome, Selective antibody deficiency with normal immunoglobulins, Selective cobalamin malabsorption with proteinuria, Semilobar holoprosencephaly and primary craniosynostosis, Sensitization to 2-hydroxyethyl methacrylate, Sensorimotor neuropathy with ataxia autosomal dominant, Sensorineural deafness and male infertility, Sensorineural deafness with imperforate anus and hypoplastic thumbs, Sensorineural deafness, hypospadias, and synostosis of metacarpals and metatarsals 4 and 5, Sensorineural deafness, profound, with or without a conductive component, associated with a unique developmental abnormality of the ear, Sensorineural hearing loss, enamel hypoplasia, and nail abnormalities, Septic phlebitis of the internal jugular vein, Septo-optic dysplasia with digital anomalies, Septo-optic dysplasia with growth hormone deficiency, Serine pyruvate aminotransferase deficiency, Serpentine fibula-polycystic kidneys syndrome, SERPINFI- related osteogenesis imperfecta, Severe achondroplasia with developmental delay and acanthosis nigricans, Severe achondroplasia-developmental delay-acanthosis nigricans syndrome, Severe childhood autosomal recessive muscular dystrophy, North African type, Severe combined immunodeficiency due to ADA deficiency, Severe combined immunodeficiency due to adenosine deaminase deficiency, Severe combined immunodeficiency due to FOXN1 deficiency, Severe combined immunodeficiency due to ZAP70 deficiency, Severe combined immunodeficiency T- B+ due to gamma chain deficiency, Severe combined immunodeficiency T- B+, X-linked, Severe combined immunodeficiency with hypereosinophilia, Severe combined immunodeficiency with leukopenia, Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency, Severe combined immunodeficiency, HLA class ii-negative, Severe combined immunodeficiency, X-linked, Severe combined immunodeficiency, X-linked, T cell-negative, B cell-positive, NK cell-negative, Severe dental aberrations in familial steroid dehydrogenase deficiency, Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome, Severe growth retardation, developmental delay with hypotonia, hypotrophy of the distal extremities, dental anomalies, and eczematous skin, Severe hereditary thrombophilia due to congenital protein C deficiency, Severe immunodeficiency, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive, Severe infantile axonal neuropathy with respiratory failure, Severe intellectual disability and progressive spastic paraplegia, Severe intellectual disability-aplasia/hypoplasia of thumb and hallux syndrome, Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome, Severe 'knock-knees' and variable lesser malalignment at the elbows and wrists, Severe mental deficiency proportionate dwarfism and delayed sexual maturation, Severe mental retardation, microcephaly, long narrow face, ocular anomalies, and long thin hands and feet, Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome, Severe microcephaly and self-limiting dilated cardiomyopathy, Severe microcephaly with mental retardation and dilated cardiomyopathy, Severe MPS I (subtype, also known as Hurler syndrome), Severe muscle pain and abnormally high eosinophils, Severe or complete loss of motor function in the lower extremities and lower portions of the trunk, Severe refractory status epilepticus owing to presumed encephalitis, Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism, Severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome, Severe thrombocytopenia and selective, marked decrease or absence of megakaryocytes, Severe ulnar aplasia and lobster claw feet, Severe upper limb brachymesomelia, glomerulocystic renal dysplasia, cranial and facial abnormalities, corneal opacities, Severe upper limb hypoplasia and Mullerian duct anomalies, Sex reversion-kidneys, adrenal and lung dysgenesis syndrome, Sex-linked mental retardation, short stature, obesity and hypogonadism, Sexual precocity, familial, gonadotropin-independent, SH2D1A-Related Lymphoproliferative Disease, X-Linked, Shashi X-linked mental retardation syndrome, Short branched-chain acyl-CoA dehydrogenase deficiency, Short foot/brachydactyly of toes, camptodactyly , brachydactyly, Short limb dwarfism with saddle nose, spinal alterations, and metaphyseal striation, Short limbed dwarfism with extensive stippling, Short rib polydactyly syndrome Beemer-Langer type, Short rib polydactyly syndrome Verma Naumoff type, Short rib-polydactyly syndrome Beemer type, Short rib-polydactyly syndrome Majewski type, Short rib-polydactyly syndrome Saldino-Noonan type, Short ribs, polysyndactyly, cranial synostosis, cleft palate cardiovascular and urogenital anomalies and severe ossification defect, Short stature heart defect and craniofacial anomalies, Short stature mental retardation type I preaxial polydactyly with colobomatous abnormalities, Short stature unique facies enamel hypoplasia progressive joint stiffness and high-pitched voice, Short stature with delayed bone age, expressive language delay, a triangular face with a prominent nose and deep-set eyes, Short stature, abnormal face, joint laxity, hernias, delayed bone age, and severe psychomotor retardation, Short stature, brachydactyly, nail dysplasia and mental retardation, Short stature, characteristic facies, macrodontia, mental retardation, and skeletal anomalies, Short stature, congenital optic atrophy, and hypoplasia of the cervical vertebral bodies and distal phalanges, Short stature, facial dysmorphism, severe brachydactyly and syndactyly, Short stature, Hyperextensibility, Hernia, Ocular depression, Rieger anomaly and Teething delay, Short stature, intellectual disability, facial dysmorphism, short webbed neck, skin changes and congenital heart disease, Short stature, mental retardation and multiple dysmorphisms, Short stature, pituitary and cerebellar defects and small sella turcica, Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot, Short stature, small head circumference, sloping forehead, hearing loss, cupped ears and small testes, Short stature, webbed neck, heart disease, Short stature-pituitary and cerebellar defects-small sella turcica syndrome, Short-chain acyl-coenzyme A dehydrogenase deficiency, Short-chain enoyl-CoA hydratase deficiency, Short-lasting, Unilateral, Neuralgiform headache attacks with Conjunctival injection and Tearing, Short-rib thoracic dysplasia 6 with or without polydactyly, Shoulder and girdle defects-familial intellectual disability syndrome, Sickle cell disease associated with an other hemoglobin anomaly, Sickle cell-beta-thalassemia disease syndrome, Sickle cell-hemoglobin C disease syndrome, Sickle cell-hemoglobin D disease syndrome, Sickle cell-hemoglobin E disease syndrome, SICRET (small infarction of cochlear, retinal, and encephalic tissue) syndrome, Sideroblastic anemia and mitochondrial myopathy, Sideroblastic anemia with marrow cell vacuolization and exocrine pancreatic dysfunction (formerly), Sideroblastic anemia with spinocerebellar ataxia, Sinonasal eosinophilic angiocentric fibrosis, Sinus histiocytosis with massive lymphadenopathy, Situs inversus, complex cardiac defects, and splenic defects, X-linked, Situs inversus, cystic dysplastic kidney and pancreas, bowed lower limbs ,severe intrauterine growth retardation, and oligohydramnios, Sjogren-Larsson-like ichthyosis without CNS or eye involvement, Skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficulties, Skeletal abnormalities, Cutis laxa, craniostenosis, Ambiguous genitalia, Retardation, and Facial abnormalities, Skeletal dysplasia Jequier-Kozlowski type, Skeletal dysplasia lethal with gracile bones, Skeletal dysplasia related to campomelic dysplasia, Skeletal dysplasia with amelogenesis imperfecta and platyspondyly, Skin mastocytosis hearing loss microcephaly mild dysmorphic features and severe mental retardation, SLC6A3-Related Dopamine Transporter Deficiency Syndrome, Slow channel congenital myasthenic syndrome, Small benign fibrovascular tumor of the dermal part of the hair disk, Small cell carcinoma of the urinary bladder, Small Cell Neuroendocrine Carcinoma of the Lung, Small cell variant of anaplastic large cell lymphoma, SMD with with bowed forearms and facial dysmorphism, Smed short limb-abnormal calcification type, Snowflake degeneration in hereditary vitreoretinal degeneration, Solitary median maxillary central incisor, Solitary median maxillary central incisor syndrome, Somatostatin-secreting pancreatic neoplasm, Sorsby's pseudoinflammatory macular dystrophy, Sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay, Sparse hair, short stature, hypoplastic thumbs, single upper central incisor and abnormal skin pigmentation, Spastic ataxia, macular corneal dystrophy, congenital cataracts, myopia and vertically oval temporally tilted discs, Spastic paralysis, infantile onset ascending, Spastic paraparesis, childhood-onset, with distal muscle wasting, Spastic paraplegia - intellectual deficit - thin corpus callosum, Spastic paraplegia - nephritis - deafness, Spastic paraplegia 20, autosomal recessive, Spastic paraplegia 31, autosomal dominant, Spastic paraplegia 35, autosomal recessive, Spastic paraplegia 51, autosomal recessive, Spastic paraplegia and pigmentary abnormalities, Spastic paraplegia and retinal degeneration, Spastic paraplegia associated with brachydactyly type E, Spastic paraplegia vitiligo premature graying and characteristic facies, Spastic paraplegia with amyotrophy of hands and feet, Spastic paraplegia with iron deposits in basal ganglia, Spastic paraplegia, autosomal recessive, Troyer type, Spastic paraplegia, bilateral sensorineural deafness, intellectual retardation, and progressive nephropathy, Spastic quadriplegia-retinitis pigmentosa-intellectual disability syndrome, Spastic quadriplegia-thin corpus callosum-progressive postnatal microcephaly syndrome, Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, Speckled hyperpigmentation, palmo-plantar punctate keratoses and childhood blistering, Speech and language disorder with orofacial dyspraxia, Sphenoethmoidal encephalomeningocele agenesis of the corpus callosum and cleft lip/palate, Spinal disc herniation with autosomal recessive spastic paraplegia, Spinal muscular atrophy juvenile nonprogressive, Spinal muscular atrophy with progressive myoclonic epilepsy, Spinal muscular atrophy, distal, autosomal recessive, 1, Spinal muscular atrophy, lower extremity-predominant 1, AD, Spinal muscular atrophy, lower extremity-predominant 1, dominant, Spinal muscular atrophy, lower extremity-predominant 2, autosomal dominant, Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant, Spinal muscular atrophy, mild childhood and adolescent form, Spinal muscular atrophy, proximal, adult, autosomal recessive, Spindle cell rhabdomyosarcomas (type of ERMS), Spinocerebellar ataxia associated amyotrophy of the hands and sensorineural deafness, Spinocerebellar ataxia autosomal dominant with sensory axonal neuropathy, Spinocerebellar ataxia infantile with sensory neuropathy, Spinocerebellar ataxia with axonal neuropathy, Spinocerebellar ataxia with axonal neuropathy type 1, Spinocerebellar ataxia with axonal neuropathy type 2, Spinocerebellar ataxia with blindness and deafness, Spinocerebellar ataxia with saccadic intrusions, Spinocerebellar ataxia with slow eye movements, Spinocerebellar ataxia, autosomal recessive 2, Spinocerebellar degeneration corneal dystrophy, Spinocerebellar degeneration with macular corneal dystrophy, congenital cataracts, and myopia, Spinocerebellar degeneration with slow eye movements, Splenogonadal fusion limb defects syndrome, Split hand deformity-mandibulofacial dysostosis, Split hand split foot mandibular hypoplasia, Split-foot deformity with ectrodactyly and mandibulofacial dysostosis, Split-hand with obstructive uropathy, spina bifida, and diaphragmatic defects, Split-hand/foot malformation with long bone deficiency, Spondylar and nasal alterations with striated metaphyses, Spondylocostal dysostosis 1 autosomal recessive, Spondylocostal dysostosis 2, autosomal recessive, Spondylocostal dysostosis 3, autosomal recessive, Spondylocostal dysostosis 4, autosomal recessive, Spondylocostal dysostosis 6, autosomal recessive, Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification, Spondyloepimetaphyseal dysplasia Matrilin-3 type, Spondyloepimetaphyseal dysplasia with joint laxity, Spondyloepimetaphyseal dysplasia with multiple dislocations Hall type, Spondyloepimetaphyseal dysplasia with multiple dislocations leptodactylic type, Spondyloepimetaphyseal dysplasia, Missouri type, Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome, Spondyloepiphseal dysplasia, retinal dystrophy and antibody deficiency, Spondyloepiphyseal dysplasia nephrotic syndrome, Spondyloepiphyseal dysplasia pseudoachondroplastic 2, Spondyloepiphyseal dysplasia tarda - progressive arthropathy, Spondyloepiphyseal dysplasia tarda with progressive arthropathy, Spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome, Spondyloepiphyseal dysplasia with congenital joint dislocations, Spondyloepiphyseal dysplasia with congenital joint dyslocations, CHST3 type, Spondyloepiphyseal dysplasia, congenital type, Spondyloepiphyseal dysplasia, Maroteaux type, Spondyloepiphyseal dysplasia, pseudoachondroplastic, Spondylometaepiphyseal dysplasia Anauxetic type, Spondylometaepiphyseal dysplasia Menger type, Spondylometaepiphyseal dysplasia short limb-abnormal calcification type, Spondylometaphyseal dysplasia Richmond type, Spondylometaphyseal dysplasia Schmidt type, Spondylometaphyseal dysplasia Sutcliffe type, Spondylometaphyseal dysplasia with enchondromatous changes, Spondylometaphyseal dysplasia with severe genu valgum, Spondyloperipheral dysplasia with short ulna, Spongy degeneration of the central nervous system, Spontaneous occlusion of the circle of Willis, Spontaneous periodic hypothermia syndrome, Spontaneous recurrent hypothermia syndrome, Static encephalopathy of childhood with neurdegeneration in adulthood, STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD, Status epilepticus owing to presumed encephalitis, Sternal nonunion with supraumbilical raphe, Steroid-responsive encephalopathy associated with autoimmune thyroiditis, Stevens-Johnson syndrome toxic epidermal necrolysis spectrum, Stiff person syndrome and related disorders, Straight-chain Acyl-CoA oxidase deficiency, Strasburger-Hawkins-Eldridge-Hargrave-McKusick syndrome, Stress-induced polymorphic ventricular tachycardia, Striopallidodentate calcinosis autosomal dominant adult-onset, Stuve-Wiedemann/Schwartz-Jampel type 2 syndrome, STXBP1-related early-onset encephalopathy, Subacute necrotizing encephalomyelopathy maternally inherited, Subacute spongiform encephalopathy, Gerstmann-Straussler type, Subcortical vascular encephalopathy, progressive, Subglottic bar, congenital heart disease and low stature, Submandibular, ocular, and rectal pain with flushing, Succinyl-CoA acetoacetate transferase deficiency, Succinyl-CoA:3-oxoacid CoA transferase deficiency, SUCLA2-Related Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form with Methylmalonic Aciduria, Sucrase-isomaltase deficiency, congenital, Sucrose-isomaltase malabsorption, congenital, Sudden infant death - dysgenesis of the testes, Sudden infant death-dysgenesis of the testes syndrome, Sudden onset of unilateral flushing and sweating, Sudden unexpected nocturnal death syndrome, Superficial annular corneal dystrophy, ichthyosis nigrans, microcephaly and mild mental subnormality, Superior oblique oculomotor palsy, familial congenital, Supratentorial Embryonal Tumor, Not Otherwise Specified, Supratentorial primitive neuroectodermal tumors, childhood, Supravalvar aortic stenosis, Eisenberg type, Susceptibility to acute infection-induced encephalopathy-3, Susceptibility to acute necrotizing encephalopathy, Susceptibility to Infection-Induced Acute Encephalopathy 3, Susceptibility to severe cutaneous adverse reaction ITY TO, Sutcliffe type of spondylometaphyseal dysplasia, Sutherland-Haan X-linked intellectual disability syndrome, SWS type I - Facial and leptomeningeal angiomas, SWS type II - Facial angioma alone, no CNS involvement, SWS type III - Isolated leptomeningeal angiomas, Symmetric dyschromatosis of the extremities, Symphalangism, short stature, skeletal anomalies, and accessory testis, Syndactyly mesoaxial synostotic with phalangeal reduction, Syndactyly type I with microcephaly and mental retardation, Syndactyly with associated metacarpal and metatarsal fusion, Syndactyly, preaxial polydactyly and sternal deformity, Syndactyly, telecanthus, anogenital and renal malformations, Syndactyly-ectodermal dysplasia-cleft/lip palate, Syndermotic cataract and congenital ichthyosis, Syndrome of dwarfism, mental retardation, lens opacities, nystagmus, strabismus, cryptorchidism and absent patellae, Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria, Syndrome of inappropriate antidiuretic hormone secretion, Syndrome of microcephaly, deafness/malformed ears, mental retardation and peculiar facies, Syndrome of microtia and aortic arch anomalies, Syndrome of polyneuropathy, skin hyperpigmentation, oedema and hepatosplenomegaly, Syndrome of tetraamelia with pulmonary hypoplasia, Syndrome of transient headache and neurological deficits with cerebrospinal fluid lymphocytosis: HaNDL, Syndrome of unilobed or absent thymus, renal and ureter agenesis/dysgenesis, and intrauterine growth retardation (IUGR), Syndrome of widened medullary cavities of the metacarpals and phalanges, aortic calcification and abnormal dentition, Syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart, Syndrome with triphalangia of thumbs, thrombasthenia Glanzmann and deafness of internal ear, Syndromic diarrhea/Tricho-hepato-enteric syndrome, SYNE1-related autosomal recessive cerebellar ataxia, Syngap1 Gene Mutation Linked To Intellectual Disability, Schizophrenia and Autism, Synovitis acne pustulosis hyperostosis osteitis, Synovitis granulomatous with uveitis and cranial neuropathies, Synovitis, Acne, Pustlosis, Hyperostosis, and Osteomyelitis, Systemic hemosiderosis due to aceruloplasminemia, Systemic IgG4-related plasmacytic syndrome, Systemic IgG4-related sclerosing syndrome, Systemic onset juvenile rheumatoid arthritis, Systemic-onset juvenile idiopathic arthritis, Office of Rare Disease Research Facebook Page, Office of Rare Disease Research on Twitter, U.S. Department of Health & Human Services, Caring for Your Patient with a Rare Disease, Preguntas Más Frecuentes Sobre Enfermedades Raras, Como Encontrar un Especialista en su Enfermedad, Consejos Para una Condición no Diagnosticada, Consejos Para Obtener Ayuda Financiera Para Una Enfermedad, Preguntas Más Frecuentes Sobre los Trastornos Cromosómicos, Sacral hemangiomas multiple congenital abnormalities, Sacral meningocele conotruncal heart defects, Dandy-Walker malformation with sagittal craniosynostosis and hydrocephalus, Woolly hair hypotrichosis everted lower lip and outstanding ears, Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia, Cardioauditory syndrome of Sanchez Cascos, Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis, Hypoparathyroidism-intellectual disability-dysmorphism syndrome, Krabbe disease atypical due to Saposin A deficiency, STING-associated vasculopathy with onset in infancy, Blepharophimosis intellectual disability syndromes, 2-methylbutyryl-CoA dehydrogenase deficiency, Spinocerebellar ataxia autosomal recessive 3, Short-chain acyl-CoA dehydrogenase deficiency, Spinocerebellar ataxia autosomal recessive with axonal neuropathy, X-linked dominant scapuloperoneal myopathy, Amyotrophy, neurogenic scapuloperoneal, New England type, Scapuloperoneal syndrome, neurogenic, Kaeser type, Spinocerebellar ataxia autosomal recessive 4, Spinocerebellar ataxia autosomal recessive 5, Spinocerebellar ataxia autosomal recessive 6, Spinocerebellar ataxia autosomal recessive 7, Spinocerebellar ataxia autosomal recessive 8, Autosomal recessive spinocerebellar ataxia 9, Corneal dystrophy crystalline of Schnyder, Slow-channel congenital myasthenic syndrome, Superior semicircular canal dehiscence syndrome, N-acetyl-alpha-D-galactosaminidase deficiency type III, Spondylometaphyseal dysplasia Algerian type, Diabetes insipidus nephrogenic mental retardation and intracerebral calcification, Schrander-Stumpel Theunissen Hulsmans syndrome, Congenital thrombotic thrombocytopenic purpura, Syndrome of inappropriate antidiuretic hormone, Thickened earlobes-conductive deafness syndrome, Severe combined immunodeficiency due to complete RAG1/2 deficiency, Severe combined immunodeficiency, atypical, Severe combined immunodeficiency with sensitivity to ionizing radiation, X-linked severe combined immunodeficiency, Palmoplantar keratoderma-sclerodactyly syndrome, Osteosclerosis with ichthyosis and premature ovarian failure, Sclerosing mucoepidermoid carcinoma with eosinophilia, Severe congenital neutropenia autosomal recessive 3, Hereditary paraganglioma-pheochromocytoma, Sebaceous gland hyperplasia, familial presenile, Congenital dyserythropoietic anemia type 2, Seckel like syndrome Majoor-Krakauer type, Spondyloepiphyseal dysplasia tarda X-linked, Spondyloepiphyseal dysplasia Maroteaux type, Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech, Microcephaly microcornea syndrome Seemanova type, Imperforate oropharynx-costo vetebral anomalies, Convulsions, benign familial infantile, 1, Spondyloenchondrodysplasia with immune dysregulation, Spondyloepimetaphyseal dysplasia Genevieve type, Spondyloepimetaphyseal dysplasia Matrilin-3 related, Spondyloepimetaphyseal dysplasia Missouri type, Spondyloepimetaphyseal dysplasia Shohat type, Spondyloepimetaphyseal dysplasia X-linked, Spondyloepimetaphyseal dysplasia, Aggrecan type, Spondyloepimetaphyseal dysplasia joint laxity, Beta-Propeller Protein-Associated Neurodegeneration, 2-hydroxyethyl methacrylate sensitization, Progressive familial intrahepatic cholestasis type 2, Progressive familial intrahepatic cholestasis 1, T-cell immunodeficiency, congenital alopecia and nail dystrophy, Severe congenital neutropenia autosomal dominant, Steroid dehydrogenase deficiency dental anomalies, Severe generalized recessive dystrophic epidermolysis bullosa, Spinal muscular atrophy with respiratory distress 1, AP-4-Associated Hereditary Spastic Paraplegia, GATAD2B-associated neurodevelopmental disorder, Severe intellectual disability-progressive spastic diplegia syndrome, Intellectual disability - athetosis - microphthalmia, Febrile infection-related epilepsy syndrome, Acquired amegakaryocytic thrombocytopenia, Ulnar hypoplasia lobster claw deformity of feet, Severe X-linked intellectual disability, Gustavson type, X-linked intellectual disability - short stature – obesity, Isolated growth hormone deficiency type 1A, Fundus dystrophy, pseudoinflammatory, of Sorsby, Splenogonadal fusion limb defects micrognatia, Sphingosine phosphate lyase insufficiency syndrome, X-linked lymphoproliferative disease due to SH2D1A deficiency, Alopecia, epilepsy, pyorrhea, mental subnormality, Spondyloepimetaphyseal dysplasia Sponastrime type, Short-limb skeletal dysplasia with severe combined immunodeficiency, Short rib-polydactyly syndrome, Majewski type, Short stature deafness neutrophil dysfunction, Short stature with optic atrophy and Pelger-Huët anomaly syndrome, X-linked intellectual disability, Abidi type, Short stature-craniofacial anomalies-genital hypoplasia syndrome, Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency, Short-lasting unilateral neuralgiform headache attacks with cranial autonomic symptoms, Shoulder girdle defect mental retardation familial, Shprintzen-Goldberg craniosynostosis syndrome, Sudden infant death with dysgenesis of the testes syndrome, X-linked intellectual disability, Siderius type, Mitochondrial myopathy and sideroblastic anemia, Sideroblastic anemia pyridoxine-refractory autosomal recessive, Sideroblastic anemia pyridoxine-responsive autosomal recessive, Anemia sideroblastic and spinocerebellar ataxia, Situs inversus totalis with cystic dysplasia of kidneys and pancreas, Sjogren's syndrome, juvenile, secondary to autoimmune disease, Stevens-Johnson syndrome/toxic epidermal necrolysis, Spondylometaphyseal dysplasia, Kozlowski type, Pierre Robin sequence with pectus excavatum and rib and scapular anomalies, Skin fragility-woolly hair-palmoplantar keratoderma syndrome, Mastocytosis cutaneous with short stature conductive hearing loss and microtia, Early infantile epileptic encephalopathy 25, Histiocytosis-lymphadenopathy plus syndrome, SLC4A1-associated distal renal tubular acidosis, Spinal muscular atrophy type 1 with congenital bone fractures, Autosomal dominant spinal muscular atrophy, lower extremity-predominant 1, Autosomal dominant spinal muscular atrophy, lower extremity-predominant 2, Spinal muscular atrophy-progressive myoclonic epilepsy syndrome, Spondyloepimetaphyseal dysplasia Strudwick type, Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism, Spondylometaphyseal dysplasia with cone-rod dystrophy, Spondylometaepiphyseal dysplasia short limb-hand type, Autosomal dominant compelling helio ophthalmic outburst syndrome, Insulin-like growth factor 1 resistance to, Aniridia renal agenesis psychomotor retardation, Coloboma of macula with type B brachydactyly, Thumb deformity, alopecia, pigmentation anomaly, Spastic angina with healthy coronary artery, Infantile-onset ascending hereditary spastic paralysis, Fatty acid hydroxylase-associated neurodegeneration, Spastic paraplegia facial cutaneous lesions, Spastic paraplegia neuropathy poikiloderma, Spastic paraplegia with precocious puberty, Spastic paraplegia-epilepsy-intellectual disability syndrome, Spastic paraplegia-glaucoma-intellectual disability syndrome, Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome, Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome, Epidermolysis bullosa simplex with mottled pigmentation, Autosomal recessive spastic paraplegia type 49, Spinal atrophy ophthalmoplegia pyramidal syndrome, Neuropathy, distal hereditary motor, Jerash type, Spinocerebellar degeneration and corneal dystrophy, Split hand split foot malformation autosomal recessive, Split hand urinary anomalies spina bifida, Spondylodysplastic Ehlers-Danlos syndrome, Spondyloepimetaphyseal dysplasia micromelic, Spondyloepimetaphyseal dysplasia with hypotrichosis, Spondyloepimetaphyseal dysplasia with multiple dislocations, Spondyloepimetaphyseal dysplasia, Handigodu type, Spondylohypoplasia, arthrogryposis and popliteal pterygium, Spondylometaphyseal dysplasia corner fracture type, Spondylometaphyseal dysplasia East-African type, Spondylometaphyseal dysplasia Sedaghatian type, Spondylometaphyseal dysplasia with dentinogenesis imperfecta, Subcutaneous panniculitis-like T-cell lymphoma, Squamous cell carcinoma of the head and neck, Genetic steroid-resistant nephrotic syndrome, Succinic semialdehyde dehydrogenase deficiency, Craniofacial dysostosis with diaphyseal hyperplasia, Progressive deafness with stapes fixation, Supraumbilical midabdominal raphe and facial cavernous hemangiomas, Leukoencephalopathy - dystonia - motor neuropathy, Systemic onset juvenile idiopathic arthritis, Alaninuria with microcephaly, dwarfism, enamel hypoplasia and diabetes mellitus, Intellectual deficit - short stature - hypertelorism, Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence, Phocomelia ectrodactyly deafness sinus arrhythmia, Familial congenital palsy of trochlear nerve, Brachydactyly-mesomelia-intellectual disability-heart defects syndrome, Catecholaminergic polymorphic ventricular tachycardia, Early infantile epileptic encephalopathy 4, Mitochondrial DNA-associated Leigh syndrome, Subaortic stenosis short stature syndrome, Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy, Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria, Benign recurrent intrahepatic cholestasis 1, Benign recurrent intrahepatic cholestasis, Superficial siderosis of the central nervous system, Childhood Supratentorial Embryonal Tumor, Not Otherwise Specified, Supratentorial primitive neuroectodermal tumor, Symphalangism with multiple anomalies of hands and feet, Symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch, Syndactyly ectodermal dysplasia cleft lip palate hand foot, Microphthalmia with linear skin defects syndrome, SYNGAP1-related non-syndromic intellectual disability, Synostosis of talus and calcaneus short stature, Synovial chondromatosis, familial with dwarfism, Myalgic encephalomyelitis/chronic fatigue syndrome.
You will be subject to the destination website's privacy policy when you follow the link. Blood Pressure. Chronic Pain. Conditions beginning with the letter S. SAD (Seasonal Affective Disorder) SARS (Severe Acute Respiratory Syndrome, Atypical Pneumonia) Scabies (Mite Infestation, Body Lice) Schizophrenia (Psychosis, Psychotic Disorders) Sciatica. Arthritis. Read more about which diseases are included on the GARD website. Terms of Use. 3. Trusted information on medical conditions Have a health concern? Saving Lives, Protecting People, Zoonotic Diseases from Animals — see Animal-Related Diseases, Zoonotic enteric diseases — see Gastrointestinal Diseases from Animals, U.S. Department of Health & Human Services.
Cfb Finance, Powerapps For Beginners, Blowfish Mamba Wedge, Add Image To Video App, Susan Rice Benghazi, Bar Billiards Table Plans, Ancient Alphabet Symbols Nyt Crossword, Raptors Number 3, 6ft Pool Table Dining Table, Rowena Wallace Net Worth, Criterion Sale, Ali Brigginshaw Wife, Armenia Female, How Long Does It Take To Learn Russian, Mcmillions Episode 3 Watch Online, Tigger Silhouette, How Long Does It Take To Learn Russian, Embed Power Bi In Powerapps, Microsoft Power Platform Books, Exway Flex Release Date, Research Paper Template Pdf, Georgia Nature, Climbing Aconcagua Experience, Amon-ra St Brown 40, Drogheda United Under 17, Used Pool Tables For Sale In South Florida, Pick Me Up On Your Way Down Lyrics, Serie A - Fairplay Table, Pool Rules If You Hit Opponents Ball In, Class Clown Behavior, Chicago In-text Citation, Janet Jamora First Husband, Angela Southern University Division, Italian Phrases For Travel Printable, Hebrew Gematria Number Meanings, European Journal Of Mathematics, Word Picture Puzzles, Cbf Meaning, Number 7 Blue Cigarettes New Package, The Device (2014), Carlos P Garcia Accomplishments, World Matchplay Darts 2020 Draw, Magnus Carlsen Net Worth, Little Canada Toronto, Day Of The Lord Meaning, Logitech K750 Manual, Phone Ring Holder Wireless Charging, St Roch's Merchandise, Mjällby Vs Falkenberg H2h, Lean Library Alternatives, Gloria's Menu, Nobunaga Shimazaki, Adam's Mega Foam Vs Ultra Foam, Pucked Pdf, Over/under Ncaa Football 2019, Google Alert Center, Where To Buy Padron Peppers, Deshannon Berry,