Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/10
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- Saal Greenstein syndrome
- Sackey Sakati Aur syndrome
- Sacral defect anterior sacral meningocele
- Sacral hemangiomas multiple congenital abnormalities
- Sacral meningocele conotruncal heart defects
- Sacral plexopathy
- Sacrococcygeal dysgenesis association
- Saito Kuba Tsuruta syndrome
- Salcedo syndrome
- Salivary disorder
- Salivary gland disorders
- Sallis Beighton syndrome
- Salti Salem syndrome
- Sammartino Decreccio syndrome
- Samson Gardner syndrome
- Samson Viljoen syndrome
- Sanderson Fraser syndrome
- Sandhaus Ben Ami syndrome
- Sandrow Sullivan Steel syndrome
- Santos Mateus Leal syndrome
- Saul Wilkes Stevenson syndrome
- Say Barber Hobbs syndrome
- Say Barber Miller syndrome
- Say Carpenter syndrome
- Say Field Coldwell syndrome
- Scalp defects postaxial polydactyly
- Scalp ear nipple syndrome
- Scapuloiliac dysostosis
- Scapuloperoneal myopathy
- Schaap Taylor Baraitser syndrome
- Schaefer Stein Oshman syndrome
- Schamberg disease
- Schereshevskij Turner
- Scheurermann's disease
- Schimke syndrome
- Schindler disease
- Schinzel syndrome
- Schinzel-Giedion midface retraction syndrome
- Schisis association
- Schizophrenia mental retardation deafness retinitis
- Schlegelberger Grote syndrome
- Schneckenbecken dysplasia
- Schofer Beetz Bohl syndrome
- Scholte Begeer Van Essen syndrome
- Schraderman's disease
- Schrander Stumpel Theunissen Hulsmans syndrome
- Schroer Hammer Mauldin syndrome
- Schwartz Newark syndrome
- Schwartz-Jampel syndrome
- Schwartz-lelek syndrome
- Schweitzer Kemink Malcolm syndrome
- Scleredema
- Scleroatonic myopathy
- Sclerocornea, Syndactyly, ambiguous genitalia
- Scleromyxedema
- Sclerosing bone dysplasia mental retardation
- Sclerosing cholangitis
- Sclerosing Lymphocytic Lobulitis
- Sclerosing Mesenteritis
- Sclerosteosis
- Scoliosis as part of NF
- SCOT deficiency
- Scott Bryant Graham syndrome
- Scott syndrome
- 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
- 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
- Selig Benacerraf Greene syndrome
- Semmerkrot Haraldsson Weenaes syndrome
- Sener syndrome
- Sengers Hamel Otten syndrome
- Senior syndrome
- Senior-Loken Syndrome
- Sennetsu Fever
- Sensory radicular neuropathy recessive form
- Senter syndrome
- Seow Najjar syndrome
- Septooptic dysplasia digital anomalies
- Sequeiros Sack syndrome
- Seres Santamaria Arimany Muniz syndrome
- Setleis syndrome
- Severe Infantile Axonal Neuropathy
- Sex Chromosome Disorders
- Sharma Kapoor Ramji syndrome
- Shaver's Disease
- Shith Filkins syndrome
- 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 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
- Sialidosis type 1 and 3
- Sialuria, French type
- Siegler Brewer Carey syndrome
- Silengo Lerone Pelizzo syndrome
- Silicosiderosis
- Sillence syndrome
- Simian B virus infection
- Simosa Penchaszadeh Bustos syndrome
- Singh Chhaparwal Dhanda syndrome
- Single upper central incisor
- Single ventricular heart
- Singleton Merten syndrome
- Sinus cancer
- Sinus histiocytosis
- Sinus node disease and myopia
- Situs inversus totalis with cystic dysplasia of kidneys and pancreas
- Situs inversus viscerum-cardiopathy
- Sjogren Larsson like syndrome
- Sjogren Larsson 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
- Small non-cleaved cell lymphoma
- Smet Fabry Fryns syndrome
- Smith Fineman Myers syndrome
- Smith Martin Dodd syndrome
- Sohval Soffer syndrome
- Sommer Hines syndrome
- Sommer Rathbun Battles syndrome
- Sommer Young Wee Frye syndrome
- Sondheimer syndrome
- Sonoda syndrome
- Sosby syndrome
- Southwestern Athabaskan genetic diseases
- Sparse hair ptosis mental retardation
- 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
- Spherophakia brachymorphia syndrome
- Spina bifida hypospadias
- Spinal atrophy ophthalmoplegia pyramidal syndrome
- Spinal bulbar motor neuropathy
- Spinal bulbar muscular atrophy
- Spinal cord disorder
- 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
- Spine rigid cardiomyopathy
- Spinocerebellar ataxia amyotrophy deafness
- Spinocerebellar ataxia dysmorphism
- Spinocerebellar atrophy type 3
- Spinocerebellar degeneration corneal dystrophy
- Spinocerebellar degenerescence book type
- Spirurida Infections
- Spleen neoplasm
- Splenic agenesis syndrome
- Splenogonadal fusion limb defects micrognatia
- 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
- 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
- Spondylohypoplasia arthrogryposis popliteal pteryg
- Spondylometaphyseal dysplasia, 'corner fracture' t
- Spondylometaphyseal dysplasia, Schmidt type
- Spondylometaphyseal dysplasia, Sedaghatian type
- Spondylometaphyseal dysplasia, X-linked
- Spondyloperipheral dysplasia short ulna
- Spongy degeneration of central nervous system
- Spontaneous periodic hypothermia
- Spontaneous pneumothorax familial type
- Spranger schinzel yers syndrome
- SSADH (succinic semialdehyde dehydrogenase deficiency)
- SSPE (subacute sclerosing panencephalitis)
- Stalker chitayat syndrome
- Stampe sorensen syndrome
- Steatocystoma multiplex natal teeth
- Steele Richardson Olszewski syndrome, atypical
- Steinfeld syndrome
- 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
- Stiff skin syndrome
- 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
- Storage pool platelet disease
- Stormorken sjaastad langslet syndrome
- Stratton garcia young syndrome
- Stratton parker syndrome
- Streeter's (Amniotic Bands)
- Striatonigral degeneration infantile
- Strudwick Syndrome
- Stuart factor deficiency, congenital
- Stuccokeratosis
- Stuve Wiedemann dysplasia
- Subacute cerebellar degeneration
- Subacute sclerosing leucoencephalitis
- 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
- Succinyl-CoA acetoacetate transferase deficiency
- Sulfatidosis juvenile, Austin type
- Sulfite and xanthine oxydase deficiency
- Summitt syndrome
- Super mesenteric artery syndrome
- Supraumbilical midabdominal raphe and facial cavernous hemangiomas
- Sutherland Haan syndrome
- Sutton disease II
- Sutton's Disease II
- Swyer James and McLeod Syndrome
- Sybert Smith syndrome
- 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
- 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-polydactyly-ear lobe syndrome
- Syngnathia cleft palate
- Syngnathia multiple anomalies
- Synostosis of talus and calcaneus short stature
- Synovial cancer
- Synovialosarcoma
- Synovitis acne pustulosis hyperostosis osteitis
- Synovitis granulomatous uveitis cranial neuropathi
- Synpolydactyly
- Syphilis embryopathy
- Syringocystadenoma papilliferum
- Syringomas natal teeth oligodontia
- Syringomelia hyperkeratosis
- Systemic arterio-veinous fistula
- Systemic necrotizing angeitis
- T cell immunodeficiency primary
- Tabatznik syndrome
- Tamari Goodman syndrome
- Tang Hsi Ryu syndrome
- Taste disorder
- TAU syndrome
- Taurodontia absent teeth sparse hair
- Taybi Linder syndrome
- Taybi syndrome
- Teebi Kaurah syndrome
- Teebi Naguib Alawadi syndrome
- Teebi Shaltout syndrome
- Teebi syndrome
- Teeth noneruption of with maxillary hypoplasia and genu valgum
- Tel Hashomer camptodactyly syndrome
- Telangiectasia ataxia variant V1
- Telecanthus hypertelorism pes cavus
- Telecanthus with associated abnormalities
- Telencephalic leukoencephalopathy
- Telfer Sugar Jaeger syndrome
- Temporomandibular ankylosis
- Temporomandibular joint dysfunction (TMJ)
- Temtamy Shalash syndrome
- Ter Haar Hamel Hendricks syndrome
- Ter Haar syndrome
- Teratocarcinosarcoma
- Tethered spinal cord disease
- Tetraamelia ectodermal dysplasia
- Tetraamelia multiple malformations
- Tetraamelia pulmonary hypoplasia
- Tetraamelia-syrinx
- Tetrahydrobiopterin deficiencies
- Tetrasomy X
- Thakker Donnai syndrome
- Thalamic degeneration symmetrical infantile
- Thalamic degenerescence infantile
- Thanatophoric dysplasia cloverleaf skull
- Thanatophoric dysplasia Glasgow variant
- Thanos Stewart Zonana syndrome
- Theodor Hertz Goodman syndrome
- Thiele syndrome
- Thiemann epiphyseal disease
- Thies Reis syndrome
- Thin ribs tubular bones dysmorphism
- Thiolase deficiency
- Thiopurine S methyltranferase deficiency
- Thomas Jewett Raines syndrome
- Thomas syndrome
- Thombocytopenia X linked
- Thompson Baraitser syndrome
- Thong Douglas Ferrante syndrome
- Thoracic celosomia
- Thoracic dysplasia hydrocephalus syndrome
- Thoraco abdominal enteric duplication
- Thoraco limb dysplasia Rivera type
- Thoracolaryngopelvic dysplasia
- Thoracopelvic dysostosis
- Thost-Unna palmoplantar keratoderma
- Thrombocytopathy asplenia miosis
- Thrombocytopenia cerebellar hypoplasia short stature
- Thrombocytopenia chromosome breakage
- Thrombocytopenia multiple congenital anomaly
- Thrombocytopenia Robin sequence
- Thrombomodulin anomalies, familial
- Thumb absence hypoplastic halluces
- Thumb absent short stature immune deficiency
- Thumb deformity, alopecia, pigmentation anomaly
- Thumb deformity
- Thumb stiff brachydactyly mental retardation
- Thymic epithelial tumor
- Thymic renal anal lung dysplasia
- Thymus neoplasm
- Thyrocerebrorenal syndrome
- Thyroid agenesis
- Thyroid hormone plasma membrane transport defect
- Thyroid, renal and digital anomalies
- Tièche-Jadassohn nevus
- Tibia absent polydactyly arachnoid cyst
- Tibiae bowed radial anomalies osteopenia fracture
- Tibial aplasia ectrodactyly hydrocephalus
- Tibial aplasia ectrodactyly
- Tibial hemimelia cleft lip palate
- Tollner Horst Manzke syndrome
- Toluene antenatal infection
- Tomaculous neuropathy
- Tome Brune Fardeau syndrome
- Toni Debre Fanconi maladie
- Toni-Fanconi syndrome
- Toriello Carey syndrome
- Toriello Lacassie Droste syndrome
- Toriello syndrome
- Toriello-Higgins-Miller syndrome
- Torres Ayber syndrome
- Torsion dystonia 7
- Torticollis keloids cryptorchidism renal dysplasia
- Tosti Misciali Barbareschi syndrome
- Total Hypotrichosis, Mari type
- Toxic conjunctivitis
- Toxopachyoteose diaphysaire tibio peroniere
- Toxoplasmosis congenital
- Tracheal agenesis
- Tracheobronchomalacia
- Tracheobronchopathia osteoplastica
- Tracheoesophageal fistula symphalangism
- Tracheophageal fistula hypospadias
- Tranebjaerg Svejgaard syndrome
- Transcobalamin II deficiency
- Transient neonatal arthrogryposis
- Transplacental infections
- Transverse limb deficiency hemangioma
- TRAPS (TNF-receptor-associated periodic syndrome)
- Treft Sanborn Carey syndrome
- Trevor disease
- Triatrial heart
- Tricho dento osseous syndrome type 1
- Tricho odonto onycho dermal syndrome
- Tricho odonto onychodysplasia syndactyly dominant type
- Tricho onychic dysplasia
- Tricho onycho hypohidrotic dysplasia
- Tricho retino dento digital syndrome
- Trichodental syndrome
- Tricho-dento-osseous syndrome
- Trichodermodysplasia dental alterations
- Trichodysplasia xeroderma
- Trichoepithelioma multiple familial
- Trichofolliculloma
- Tricho-hepato-enteric syndrome
- Trichomalacia
- Trichomegaly cataract hereditary spherocytosis
- Trichomegaly retina pigmentary degeneration dwarfi
- Trichoodontoonychial dysplasia
- Trichorhinophalangeal syndrome type I
- Trichorhinophalangeal syndrome type II
- Trichorhinophalangeal syndrome type III
- Trichostasis spinulosa
- Trichothiodystrophy sun sensitivity
- Tricuspid dysplasia
- Trigonocephaly bifid nose acral anomalies
- Trigonocephaly broad thumbs
- Trigonocephaly ptosis coloboma
- Trigonocephaly ptosis mental retardation
- Trigonomacrocephaly tibial defect polydactyly
- Trihydroxycholestanoylcoa oxidase isolated deficiency
- Trimethadione antenatal infection
- Triopia
- Triose phosphate-isomerase deficiency
- Triphalangeal thumb non opposable
- Triphalangeal thumb polysyndactyly syndrome
- Triphalangeal thumbs brachyectrodactyly
- Trismus pseudocamptodactyly syndrome
- Trisomy 1 mosaicism
- Trisomy 11 mosaicism
- Trisomy 12 mosaicism
- Trisomy 14 mosaicism
- Trisomy 2 mosaicism
- Trisomy 3 mosaicism
- Trisomy 6
- Trochlear dysplasia
- Tropical Spastic Paraparesis
- Troyer syndrome
- Trueb Burg Bottani syndrome
- Tsao Ellingson syndrome
- Tsukahara Azuno Kajii syndrome
- Tsukahara Kajii syndrome
- Tsukuhara syndrome
- Tuberculous uveitis
- Tuberous Sclerosis, type 1
- Tuberous Sclerosis, type 2
- Tucker syndrome
- Tuffli Laxova syndrome
- Tufted angioma
- Tunglang Savage Bellman syndrome
- Turner Kieser syndrome
- Turner Morgani Albright
- Turner-like syndrome
- Tutuncuoglu syndrome
- Tyrosine-oxidase temporary deficiency
