Diseases — S
64 diseases in this group. Each links to a full page: the emergence switch, the forced corrective direction, mapped agents, and the firewall. Direction only — no dose.
- Saethre-Chotzen syndromeHOLD · ↓ DOWN · restore by supplyTWIST1
- Salla disease / free sialic acid storageHOLD · ↓ DOWN · restore by supplySLC17A5
- Sandhoff diseaseNOVEL · ↓ DOWN · restore by supplyHEXB
- STING-associated vasculopathy with onset in infancyHOLD · ↑ UP · restore by clearSTING1
- SCARHOLD · ↓ DOWN · restore by supplyANO10
- Schimke immuno-osseous dysplasiaHOLD · ↓ DOWN · restore by supplySMARCAL1
- Schindler diseaseHOLD · ↓ DOWN · restore by supplyNAGA
- Schinzel-GiedionHOLD · ↑ UP · restore by clearSETBP1
- Metaphyseal chondrodysplasia, Schmid typeHOLD · ↑ UP · restore by clearCOL10A1
- Severe combined immunodeficiency, JAK3-deficientHOLD · ↓ DOWN · restore by supplyJAK3
- Severe combined immunodeficiency, RAG1-deficientHOLD · ↓ DOWN · restore by supplyRAG1
- SclerosteosisHOLD · ↑ UP · restore by clearSOST
- SCN2A encephalopathy OMIM 613721MATCH · ↑ UP · restore by clearSCN2A
- Non-dystrophic myotonia and periodic paralysisMATCH · ↑ UP · restore by clearSCN4A
- SCN8A encephalopathy OMIM 614558MATCH · ↑ UP · restore by clearSCN8A
- Severe congenital neutropenia / Kostmann diseaseMATCH · ↓ DOWN · restore by supplyHAX1
- Scott syndromeHOLD · ↓ DOWN · restore by supplyANO6
- Seckel syndromeHOLD · ↓ DOWN · restore by supplyATR
- Spondyloepiphyseal dysplasia congenitaHOLD · ↓ DOWN · restore by supplyCOL2A1
- Sengers syndromeHOLD · ↓ DOWN · restore by supplyAGK
- Senior-Loken syndrome type 5HOLD · ↓ DOWN · restore by supplyIQCB1
- Senior-LokenHOLD · ↓ DOWN · restore by supplyNPHP4
- Sepiapterin reductase deficiencyMATCH · ↓ DOWN · restore by supplySPR
- Septo-optic dysplasiaHOLD · ↓ DOWN · restore by supplyHESX1
- Serine deficiencyMATCH · ↓ DOWN · restore by supplyPHGDH
- SETD5 disorder OMIM 615761HOLD · ↓ DOWN · restore by supplySETD5
- Severe congenital neutropeniaMATCH · ↓ DOWN · restore by supplyELANE
- Surfactant protein B deficiencyHOLD · ↓ DOWN · restore by supplySFTPB
- Surfactant protein C dysfunctionHOLD · ↑ UP · restore by clearSFTPC
- Shwachman-Diamond syndromeHOLD · ↓ DOWN · restore by supplySBDS
- SialidosisHOLD · ↓ DOWN · restore by supplyNEU1
- Sickle cell disease OMIM 603903MATCH · ↓ DOWN · restore by clearHBB
- Sideroblastic anemia type 2HOLD · ↓ DOWN · restore by supplySLC25A38
- SitosterolaemiaMATCH · ↑ UP · restore by clearABCG5
- Sjogren-Larsson syndromeHOLD · ↓ DOWN · restore by supplyALDH3A2
- SLC13A5 epilepsy OMIM 615905HOLD · ↓ DOWN · restore by supplySLC13A5
- SLC35A2-CDGHOLD · ↓ DOWN · restore by supplySLC35A2
- SLC6A1-related epileptic encephalopathyHOLD · ↓ DOWN · restore by supplySLC6A1
- SMARCA4 Coffin-Siris OMIM 614609HOLD · ↓ DOWN · restore by supplySMARCA4
- SMARCB1 Coffin-Siris OMIM 614608HOLD · ↓ DOWN · restore by supplySMARCB1
- Smith-Lemli-Opitz syndromeMATCH · ↓ DOWN · restore by supplyDHCR7
- SOD1 amyotrophic lateral sclerosisMATCH · ↓ DOWN · restore by clearSOD1
- SOX11 Coffin-Siris-like OMIM 615866HOLD · ↓ DOWN · restore by supplySOX11
- Spastic paraplegia 11HOLD · ↓ DOWN · restore by supplySPG11
- Hereditary spastic paraplegia 15HOLD · ↓ DOWN · restore by supplyZFYVE26
- Spastic paraplegia 3AHOLD · ↓ DOWN · restore by supplyATL1
- HSP 4HOLD · ↑ UP · restore by clearSPAST
- Spastic paraplegia 7HOLD · ↓ DOWN · restore by supplySPG7
- Hereditary spherocytosis, recessiveHOLD · ↓ DOWN · restore by supplySPTA1
- Spinal muscular atrophyMATCH · ↓ DOWN · restore by supplySMN1
- Spondylocostal dysostosis 1HOLD · ↓ DOWN · restore by supplyDLL3
- Spondyloepiphyseal dysplasiaHOLD · ↓ DOWN · restore by supplyACAN
- SPTAN1 encephalopathy OMIM 613477HOLD · ↓ DOWN · restore by supplySPTAN1
- SRD5A3-CDGHOLD · ↓ DOWN · restore by supplySRD5A3
- Steroid-resistant nephrotic syndrome, type 2HOLD · ↓ DOWN · restore by supplyNPHS2
- Succinic semialdehyde dehydrogenase deficiencyHOLD · ↑ UP · restore by clearALDH5A1
- Stargardt diseaseHOLD · ↑ UP · restore by clearABCA4
- STAT1 GOF immunodeficiency OMIM 613796MATCH · ↑ UP · restore by clearSTAT1
- Stuve-Wiedemann syndromeHOLD · ↓ DOWN · restore by supplyLIFR
- STXBP1 encephalopathy OMIM 612164HOLD · ↓ DOWN · restore by supplySTXBP1
- Congenital sucrase-isomaltase deficiencyMATCH · ↓ DOWN · restore by supplySI
- Isolated sulfite oxidase deficiencyHOLD · ↓ DOWN · restore by supplySUOX
- Swyer syndromeHOLD · ↓ DOWN · restore by supplySRY
- SYNGAP1-related ID OMIM 612621HOLD · ↑ UP · restore by clearSYNGAP1