List of rare diseases starting with S
This list of rare diseases was originally taken from the NIH public domain resource at http://ord.aspensys.com/asp/diseases/diseases.asp .A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
- Saal Bulas syndrome
- Saal Greenstein syndrome
- Sabinas brittle hair syndrome
- Saccharopinuria
- Sackey Sakati Aur syndrome
- Sacral agenesis
- Sacral defect anterior sacral meningocele
- Sacral hemangiomas multiple congenital abnormalities
- Sacral meningocele conotruncal heart defects
- Sacral plexopathy
- Sacrococcygeal dysgenesis association
- Saethre-Chotzen syndrome
- Saito Kuba Tsuruta syndrome
- Sakati syndrome
- Salcedo syndrome
- Salivary disorder
- Salivary gland disorders
- Salla disease
- Sallis Beighton syndrome
- Salmonella Infections
- Salti Salem syndrome
- Sammartino Decreccio syndrome
- Samson Gardner syndrome
- Samson Viljoen syndrome
- Sanderson Fraser syndrome
- Sandhaus Ben Ami syndrome
- Sandhoff disease
- Sandrow Sullivan Steel syndrome
- Sanfilippo syndrome
- Santavuori disease
- Santos Mateus Leal syndrome
- SAPHO syndrome
- Sarcoidosis, pulmonary
- Sarcoidosis
- Sarcoma, Granulocytic
- Sarcosinemia
- Satoyoshi syndrome
- Saul Wilkes Stevenson syndrome
- Say Barber Hobbs syndrome
- Say Barber Miller syndrome
- Say Carpenter syndrome
- Say Field Coldwell syndrome
- Say Meyer syndrome
- Scabiophobia
- SCAD deficiency
- Scalp defects postaxial polydactyly
- Scalp ear nipple syndrome
- Scapuloiliac dysostosis
- Scapuloperoneal myopathy
- SCARF syndrome
- Schaap Taylor Baraitser syndrome
- Schaefer Stein Oshman syndrome
- Schamberg disease pigmentation disorder
- Schamberg disease
- Scheie syndrome
- Schereshevskij Turner
- Scheurermann's disease
- Schimke syndrome
- Schindler disease
- Schinzel Giedion syndrome
- Schinzel syndrome
- Schinzel-Giedion midface retraction syndrome
- Schisis association
- Schizencephaly
- Schizophrenia mental retardation deafness retinitis
- Schizophrenia, genetic types
- Schlegelberger Grote syndrome
- Schmidt syndrome
- Schmitt Gillenwater Kelly syndrome
- Schneckenbecken dysplasia
- Schofer Beetz Bohl syndrome
- Scholte Begeer Van Essen syndrome
- Schraderman's disease
- Schrander Stumpel Theunissen Hulsmans syndrome
- Schroer Hammer Mauldin syndrome
- Schwannoma, malignant
- Schwannomatosis
- Schwartz Newark syndrome
- Schwartz-Jampel syndrome
- Schwartz-lelek syndrome
- Schweitzer Kemink Malcolm syndrome
- Sciatica
- Scimitar syndrome
- Sciophobia
- Scleredema
- Scleroatonic myopathy
- Sclerocornea, Syndactyly, ambiguous genitalia
- Scleroderma
- Scleromyxedema
- Sclerosing bone dysplasia mental retardation
- Sclerosing cholangitis
- Sclerosing Lymphocytic Lobulitis
- Sclerosing Mesenteritis
- Sclerosteosis
- Sclerotylosis
- Scoleciphobia
- Scoliosis as part of NF
- Scoliosis with unilateral unsegmented bar
- Scopophobia
- SCOT deficiency
- Scotomaphobia
- Scott Bryant Graham syndrome
- Scott syndrome
- Scrapie
- Sea-blue histiocytosis
- Seafood poisoning
- Seaver Cassidy syndrome
- Sebocystomatosis
- Secernentea Infections
- Seckel like syndrome Majoor Krakauer type
- Seckel like syndrome type Buebel
- Seckel syndrome 2
- Seckel syndrome
- Secondary pulmonary hypertension
- Seemanova Lesny syndrome
- Seemanova syndrome type 2
- Seghers syndrome
- Segmental neurofibromatosis
- Segmental vertebral anomalies
- Seizures benign familial neonatal recessive form
- Seizures mental retardation hair dysplasia
- Selachophobia
- Selenium poisoning
- Selenophobia
- Selig Benacerraf Greene syndrome
- Seminoma
- Semmerkrot Haraldsson Weenaes syndrome
- Sener syndrome
- Sengers Hamel Otten syndrome
- Senior syndrome
- Senior-Loken Syndrome
- Sennetsu Fever
- Sensorineural hearing loss
- Sensory neuropathy type 1
- Sensory neuropathy
- Sensory radicular neuropathy recessive form
- Senter syndrome
- Seow Najjar syndrome
- Seplophobia
- Sepsis
- Septooptic dysplasia digital anomalies
- Septo-optic dysplasia
- Sequeiros Sack syndrome
- Seres Santamaria Arimany Muniz syndrome
- Serious digitalis intoxication
- Setleis syndrome
- Severe acute respiratory syndrome (SARS)
- Severe combined immunodeficiency
- Severe Infantile Axonal Neuropathy
- Sex Chromosome Disorders
- Sezary syndrome
- Sezary's lymphoma
- Shapiro syndrome
- Sharma Kapoor Ramji syndrome
- Sharp syndrome
- Shaver's Disease
- Sheehan syndrome
- Shigellosis
- Shith Filkins syndrome
- Shock
- Shokeir syndrome
- Short broad great toe macrocranium
- Short chain Acyl CoA dehydrogenase deficiency
- Short limb dwarf lethal Colavita Kozlowski type
- Short limb dwarf lethal Mcalister Crane type
- Short limb dwarf oedema iris coloboma
- Short limb dwarfism Al Gazali type
- Short limbs abnormal face congenital heart disease
- Short limbs subluxed knees cleft palate
- Short rib syndrome Beemer type
- Short rib-polydactyly syndrome, Beermer type
- Short rib-polydactyly syndrome, Majewski type
- Short rib-polydactyly syndrome, Saldino-Noonan type
- Short rib-polydactyly syndrome, Verma-Naumoff type
- Short rib-polydactyly syndrome
- Short ribs craniosynostosis polysyndactyly
- Short stature abnormal skin pigmentation mental retardation
- Short stature Brussels type
- Short stature contractures hypotonia
- Short stature cranial hyperostosis hepatomegaly
- Short stature deafness neutrophil dysfunction
- Short stature dysmorphic face pelvic scapula dysplasia
- Short stature heart defect craniofacial anomalies
- Short stature hyperkaliemia acidosis
- Short stature locking fingers
- Short stature mental retardation eye anomalies
- Short stature mental retardation eye defects
- Short stature microcephaly heart defect
- Short stature microcephaly seizures deafness
- Short stature monodactylous ectrodactyly cleft palate
- Short stature prognathism short femoral necks
- Short stature Robin sequence cleft mandible hand anomalies clubfoot
- Short stature talipes natal teeth
- Short stature valvular heart disease
- Short stature webbed neck heart disease
- Short stature wormian bones dextrocardia
- Short syndrome
- Short tarsus absence of lower eyelashes
- Shoulder and thorax deformity congenital heart disease
- Shoulder girdle defect mental retardation familial
- Shprintzen Golberg craniosynostosis
- Shprintzen syndrome
- Shwachman syndrome
- Shwachman-Diamond syndrome
- Shwartzman phenomenon
- Shy-Drager syndrome
- Sialadenitis
- Sialidosis type 1 and 3
- Sialidosis
- Sialuria, French type
- Sickle cell anemia
- Sickle cell crisis
- Sickle cell trait
- Sideroblastic anemia, autosomal
- Siderosis
- Siegler Brewer Carey syndrome
- Silengo Lerone Pelizzo syndrome
- Silicosiderosis
- Silicosis
- Sillence syndrome
- Silver-Russell dwarfism
- Silvery hair syndrome
- Simian B virus infection
- Simosa Penchaszadeh Bustos syndrome
- Simpson-Golabi-Behmel syndrome
- Singh Chhaparwal Dhanda syndrome
- Single upper central incisor
- Single ventricular heart
- Singleton Merten syndrome
- Sinistrophobia
- Sino-auricular heart block
- Sinus cancer
- Sinus histiocytosis
- Sinus node disease and myopia
- Sipple syndrome
- Sirenomelia
- Sitophobia
- Sitosterolemia
- Situs inversus totalis with cystic dysplasia of kidneys and pancreas
- Situs inversus viscerum-cardiopathy
- Situs inversus, X linked
- Sjogren Larsson like syndrome
- Sjogren Larsson syndrome
- Sjogren's syndrome
- Skeletal dysplasia brachydactyly
- Skeletal dysplasia epilepsy short stature
- Skeletal dysplasia orofacial anomalies
- Skeletal dysplasia San diego type
- Skeletal dysplasias
- Skeleto cardiac syndrome with thrombocytopenia
- Sketetal dysplasia coarse facies mental retardation
- Skin peeling syndrome
- Slavotinek Hurst syndrome
- Sly syndrome
- Small cell lung cancer
- Small non-cleaved cell lymphoma
- Smet Fabry Fryns syndrome
- Smith Fineman Myers syndrome
- Smith Martin Dodd syndrome
- Smith-Magenis Syndrome
- Sneddon Syndrome
- Sociophobia
- Soft tissue sarcomas
- Sohval Soffer syndrome
- Somatostatinoma
- Sommer Hines syndrome
- Sommer Rathbun Battles syndrome
- Sommer Young Wee Frye syndrome
- Somniphobia
- Sondheimer syndrome
- Sonoda syndrome
- Sophophobia
- Sosby syndrome
- Sotos syndrome
- Southwestern Athabaskan genetic diseases
- Sparse hair ptosis mental retardation
- Spasmodic dysphonia
- Spasmodic torticollis
- Spastic angina with healthy coronary artery
- Spastic ataxia Charlevoix-Saguenay type
- Spastic diplegia infantile type
- Spastic dysphonia
- Spastic paraparesis deafness
- Spastic paraparesis, infantile
- Spastic paraparesis
- Spastic paraplegia epilepsy mental retardation
- Spastic paraplegia facial cutaneous lesions
- Spastic paraplegia familial autosomal recessive form
- Spastic paraplegia glaucoma precocious puberty
- Spastic paraplegia mental retardation corpus callosum
- Spastic paraplegia nephritis deafness
- Spastic paraplegia neuropathy poikiloderma
- Spastic paraplegia type 1, X-linked
- Spastic paraplegia type 2, X-linked
- Spastic paraplegia type 3, dominant
- Spastic paraplegia type 4, dominant
- Spastic paraplegia type 5A, recessive
- Spastic paraplegia type 5B, recessive
- Spastic paraplegia type 6, dominant
- Spastic paraplegia, familial
- Spastic paresis glaucoma mental retardation
- Spastic quadriplegia retinitis pigmentosa mental retardation
- Spasticity mental retardation
- Spasticity multiple exostoses
- Spatic paraparesis vitiligo premature graying
- Spellacy gibbs watts syndrome
- Spermatogenesis arrest
- Spherocytosis
- Spherophakia brachymorphia syndrome
- Sphingolipidosis
- Spielmeyer-Vogt disease
- Spina bifida hypospadias
- Spinal atrophy ophthalmoplegia pyramidal syndrome
- Spinal bulbar motor neuropathy
- Spinal bulbar muscular atrophy
- Spinal cord disorder
- Spinal cord injury
- Spinal cord neoplasm
- Spinal dysostosis type Anhalt
- Spinal muscular atrophy type 1
- Spinal muscular atrophy type 2
- Spinal muscular atrophy type 3
- Spinal muscular atrophy type I with congenital bone fractures
- Spinal muscular atrophy
- Spinal shock
- Spinal stenosis
- Spine rigid cardiomyopathy
- Spinocerebellar ataxia 1
- Spinocerebellar ataxia 2
- Spinocerebellar ataxia 4
- Spinocerebellar ataxia 5
- Spinocerebellar ataxia 6
- Spinocerebellar ataxia 7
- Spinocerebellar ataxia 8
- Spinocerebellar ataxia amyotrophy deafness
- Spinocerebellar ataxia dysmorphism
- Spinocerebellar atrophy type 3
- Spinocerebellar degeneration corneal dystrophy
- Spinocerebellar degenerescence book type
- Spirochetes disease
- Spirurida Infections
- Spleen neoplasm
- Splenic agenesis syndrome
- Splenogonadal fusion limb defects micrognatia
- Splenomegaly
- Split hand deformity mandibulofacial dysostosis
- Split hand split foot malformation autosomal reces
- Split hand split foot mandibular hypoplasia
- Split hand split foot nystagmus
- Split hand split foot X linked
- Split hand urinary anomalies spina bifida
- Split-hand deformity
- Sponastrime dysplasia
- Spondylarthritis
- Spondylarthropathies
- Spondylarthropathy
- Spondylitis
- Spondylo camptodactyly syndrome
- Spondylo costal dysostosis dandy walker
- Spondylocarpotarsal synostosis
- Spondylocostal dysplasia dominant
- Spondylodysplasia brachyolmia
- Spondyloenchondrodysplasia
- Spondyloepimetaphyseal dysplasia congenita, Iraqi
- Spondyloepimetaphyseal dysplasia congenita, Strudw
- Spondyloepimetaphyseal dysplasia joint laxity
- Spondyloepimetaphyseal dysplasia
- Spondyloepiphyseal dysplasia nephrotic syndrome
- Spondyloepiphyseal dysplasia tarda progressive art
- Spondyloepiphyseal dysplasia tarda
- Spondyloepiphyseal dysplasia, congenital type
- Spondyloepiphyseal dysplasia
- Spondylohypoplasia arthrogryposis popliteal pteryg
- Spondylometaphyseal dysplasia, 'corner fracture' t
- Spondylometaphyseal dysplasia, Schmidt type
- Spondylometaphyseal dysplasia, Sedaghatian type
- Spondylometaphyseal dysplasia, X-linked
- Spondylometaphyseal dysplasia
- Spondyloperipheral dysplasia short ulna
- Spongiform encephalopathy
- Spongy degeneration of central nervous system
- Spontaneous periodic hypothermia
- Spontaneous pneumothorax familial type
- Sporotrichosis
- Spotted fever
- Spranger schinzel yers syndrome
- Sprengel deformity
- Squamous cell carcinoma
- SSADH (succinic semialdehyde dehydrogenase deficiency)
- SSPE (subacute sclerosing panencephalitis)
- St. Anthony's fire
- Stalker chitayat syndrome
- Stampe sorensen syndrome
- Stargardt's disease
- Steatocystoma multiplex natal teeth
- Steatocystoma multiplex
- Steele Richardson Olszewski syndrome, atypical
- Steinfeld syndrome
- Stein-Leventhal syndrome
- Stenophobia
- Sterility due to immotile flagella
- Stern lubinsky durrie syndrome
- Sternal cleft
- Sternal cyst vascular anomalies
- Sternal malformation vascular dysplasia associatio
- Steroid dehydrogenase deficiency dental anomalies
- Stevens-Johnson syndrome
- Stickler syndrome, type 1
- Stickler syndrome, type 2
- Stickler syndrome, type 3
- Stickler syndrome
- Stiff man syndrome
- Stiff skin syndrome
- Still's disease
- Stimmler syndrome
- Stoelinga de koomen davis syndrome
- Stoll alembik dott syndrome
- Stoll alembik finck syndrome
- Stoll geraudel chauvin syndrome
- Stoll kieny dott syndrome
- Stoll levy francfort syndrome
- Stomach cancer, familial
- Stomach cancer
- Storage pool platelet disease
- Stormorken sjaastad langslet syndrome
- Strabismus
- Stratton garcia young syndrome
- Stratton parker syndrome
- Streeter's (Amniotic Bands)
- Streptococcus, Group B
- Striatonigral degeneration infantile
- Strongyloidiasis
- Strudwick Syndrome
- Strumpell-lorrain disease
- Stuart factor deficiency, congenital
- Stuccokeratosis
- Sturge-Weber syndrome
- Stuve Wiedemann dysplasia
- Subacute cerebellar degeneration
- Subacute sclerosing leucoencephalitis
- Subacute sclerosing panencephalitis
- Subaortic stenosis short stature syndrome
- Subcortical laminar heterotopia
- Subependymal nodular heterotopia
- Subpulmonary stenosis
- Subvalvular aortic stenosis
- Succinate coenzyme Q reductase deficiency of
- Succinic acidemia lactic acidosis congenital
- Succinic acidemia
- Succinic semialdehyde dehydrogenase deficiency
- Succinyl-CoA acetoacetate transferase deficiency
- Sucrase-isomaltase deficiency
- Sudden infant death syndrome
- Sugarman syndrome
- Sulfatidosis juvenile, Austin type
- Sulfite and xanthine oxydase deficiency
- Sulfite oxidase deficiency
- Summitt syndrome
- Super mesenteric artery syndrome
- Supranuclear ocular palsy
- Supraumbilical midabdominal raphe and facial cavernous hemangiomas
- Suriphobia
- Susac syndrome
- Sutherland Haan syndrome
- Sutton disease II
- Sutton's Disease II
- Sweet syndrome
- Swyer James and McLeod Syndrome
- Swyer syndrome
- Sybert Smith syndrome
- Sydenham's chorea
- Symmetrical thalamic calcifications
- Symphalangism brachydactyly craniosynostosis
- Symphalangism brachydactyly
- Symphalangism Cushing type
- 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
- Syncopal paroxysmal tachycardia
- Syncopal tachyarythmia
- Syncope
- Syndactyly between 4 and 5
- Syndactyly cataract mental retardation
- Syndactyly Cenani Lenz type
- Syndactyly ectodermal dysplasia cleft lip palate hand foot
- Syndactyly type 1 microcephaly mental retardation
- Syndactyly type 2
- Syndactyly type 3
- Syndactyly type 5
- Syndactyly
- Syndactyly-polydactyly-ear lobe syndrome
- Syndrome X
- Syngnathia cleft palate
- Syngnathia multiple anomalies
- Synostosis of talus and calcaneus short stature
- Synovial cancer
- Synovial osteochondromatosis
- Synovial sarcoma
- Synovialosarcoma
- Synovitis acne pustulosis hyperostosis osteitis
- Synovitis granulomatous uveitis cranial neuropathi
- Synovitis
- Synpolydactyly
- Syphilis embryopathy
- Syphilis
- Syringobulbia
- Syringocystadenoma papilliferum
- Syringomas natal teeth oligodontia
- Syringomelia hyperkeratosis
- Syringomyelia
- Systemic arterio-veinous fistula
- Systemic carnitine deficiency
- Systemic lupus erythematosus
- Systemic mastocytosis
- Systemic necrotizing angeitis
- Systemic sclerosis
