A–Z DIRECTORY
Conditions beginning with S
- SADDANAutosomal dominant
- Saethre-Chotzen syndromeAutosomal dominant
- Sandhoff diseaseAutosomal recessive
- SATB2-associated syndromeNot inherited
- Saul-Wilson syndromeAutosomal dominant
- Scalp-ear-nipple syndromeAutosomal dominant
- Schimke immuno-osseous dysplasiaAutosomal recessive
- Schinzel-Giedion syndromeNot inherited
- Schizoaffective disorderPattern unknown
- SchizophreniaPattern unknown
- SchwannomatosisPattern unknown · Autosomal dominant
- Schwartz-Jampel syndromeAutosomal recessive
- SCN8A-related epilepsy with encephalopathyAutosomal dominant
- Seasonal affective disorderPattern unknown
- Senior-Løken syndromeAutosomal recessive
- Sepiapterin reductase deficiencyAutosomal recessive
- Septo-optic dysplasiaAutosomal dominant · Autosomal recessive
- SETBP1 haploinsufficiency disorderAutosomal dominant
- Severe congenital neutropeniaAutosomal recessive · Autosomal dominant · X-linked recessive
- Sézary syndromePattern unknown
- Sheldon-Hall syndromeAutosomal dominant
- ShinglesPattern unknown
- Short QT syndromeAutosomal dominant
- Short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delayAutosomal dominant
- Short-chain acyl-CoA dehydrogenase deficiencyAutosomal recessive
- Short/branched chain acyl-CoA dehydrogenase deficiencyAutosomal recessive
- Shprintzen-Goldberg syndromeAutosomal dominant
- Shwachman-Diamond syndromeAutosomal recessive · Autosomal dominant
- SialidosisAutosomal recessive
- SialuriaAutosomal dominant, or a new variant
- Sick sinus syndromeAutosomal recessive · Autosomal dominant
- Sickle cell diseaseAutosomal recessive
- Silver syndromeAutosomal dominant
- Silver-Russell syndromeAutosomal dominant, or a new variant
- Simpson-Golabi-Behmel syndromeX-linked
- SitosterolemiaAutosomal recessive
- Sjögren-Larsson syndromeAutosomal recessive
- Sjögren's diseasePattern unknown
- SLC35A2-congenital disorder of glycosylationX-linked dominant
- SLC4A1-associated distal renal tubular acidosisAutosomal recessive · Autosomal dominant
- Small fiber neuropathyAutosomal dominant
- Smith-Kingsmore syndromeAutosomal dominant
- Smith-Lemli-Opitz syndromeAutosomal recessive
- Smith-Magenis syndromeNot inherited
- Snijders Blok-Campeau syndromeAutosomal dominant
- Snyder-Robinson syndromeX-linked recessive
- SOST-related sclerosing bone dysplasiaAutosomal recessive
- Sotos syndromeAutosomal dominant
- Spastic paraplegia type 11Autosomal recessive
- Spastic paraplegia type 15Autosomal recessive
- Spastic paraplegia type 2X-linked
- Spastic paraplegia type 31Autosomal dominant
- Spastic paraplegia type 3AAutosomal dominant
- Spastic paraplegia type 4Autosomal dominant
- Spastic paraplegia type 49Autosomal recessive
- Spastic paraplegia type 5AAutosomal recessive
- Spastic paraplegia type 7Autosomal recessive
- Spastic paraplegia type 8Autosomal dominant, inherited or a new variant
- Spina bifidaPattern unknown
- Spinal and bulbar muscular atrophyX-linked recessive
- Spinal muscular atrophyAutosomal recessive
- Spinal muscular atrophy with lower extremity predominanceAutosomal dominant
- Spinal muscular atrophy with progressive myoclonic epilepsyAutosomal recessive
- Spinal muscular atrophy with respiratory distress type 1Autosomal recessive
- Spinocerebellar ataxia type 1Autosomal dominant
- Spinocerebellar ataxia type 2Autosomal dominant
- Spinocerebellar ataxia type 3Autosomal dominant
- Spinocerebellar ataxia type 36Autosomal dominant
- Spinocerebellar ataxia type 6Autosomal dominant
- Spondylocarpotarsal synostosis syndromeAutosomal recessive · Autosomal dominant
- Spondylocostal dysostosisAutosomal recessive · Autosomal dominant
- Spondyloenchondrodysplasia with immune dysregulationAutosomal recessive
- Spondyloepiphyseal dysplasia congenitaAutosomal dominant, or a new variant · Autosomal recessive
- Spondyloepiphyseal dysplasia with marked metaphyseal changesAutosomal dominant, or a new variant
- Spondyloepiphyseal dysplasia with metatarsal shorteningAutosomal dominant · Autosomal dominant, inherited from one affected parent
- Spondyloperipheral dysplasiaAutosomal dominant
- Spondylothoracic dysostosisAutosomal recessive
- Sporadic hemiplegic migraineAutosomal dominant · Not inherited
- SRD5A3-congenital disorder of glycosylationAutosomal recessive
- STAC3 disorderAutosomal recessive
- Stargardt macular degenerationAutosomal recessive · Autosomal dominant
- Steatocystoma multiplexAutosomal dominant
- Stevens-Johnson syndrome/toxic epidermal necrolysisNot inherited
- Stickler syndromeAutosomal dominant, or a new variant · Autosomal recessive
- STING-associated vasculopathy with onset in infancyAutosomal dominant
- Stormorken syndromeAutosomal dominant
- Sturge-Weber syndromeNot inherited
- Stüve-Wiedemann syndromeAutosomal recessive
- STXBP1 encephalopathyAutosomal dominant
- Subcortical band heterotopiaNot inherited · X-linked
- Succinic semialdehyde dehydrogenase deficiencyAutosomal recessive
- Succinyl-CoA:3-ketoacid CoA transferase deficiencyAutosomal recessive
- SUCLA2-related mitochondrial DNA depletion syndromeAutosomal recessive
- SUCLG1-related mitochondrial DNA depletion syndromeAutosomal recessive
- Sudden infant death with dysgenesis of the testes syndromeAutosomal recessive
- Supravalvular aortic stenosisAutosomal dominant
- Surfactant dysfunctionAutosomal recessive · Autosomal dominant
- Swyer syndromeAutosomal dominant · Y-linked · Autosomal recessive · Not inherited
- SYNGAP1-related intellectual disabilityAutosomal dominant
- Systemic lupus erythematosusNot inherited · Autosomal recessive
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