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Reference

Evidence

CompoundsSubstances with curated findings
OutcomesMeasured endpoints
ProteinsTransporters and enzymes
InteractionsPairs that share biology
PapersEvery paper a finding cites
ArticlesReadings of the evidence

Chemistry

ReactionsRhea and Human-GEM, by subsystem
ReachWhat a compound can become

Reference layer

PathwaysReactions grouped under one name
ProcessesWhat proteins are annotated as doing
AnatomyTissues, by what is expressed there
Cell typesCells, by what is expressed there
OrganismsSpecies a compound is prepared from
MaterialsSubstances that are not one molecule
AssessmentsRegulatory determinations, transcribed
DiseasesFeatures, genes, and where each sits

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Reference

Evidence

Compounds
Outcomes
Proteins
Interactions
Papers
Articles

Chemistry

Reactions
Reach

Reference layer

Pathways
Processes
Anatomy
Cell types
Organisms
Materials
Assessments
Diseases

Atlas Graph Twin Access

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Catalyst

Computational infrastructure for human biology, built on a provenance-aware knowledge graph. Findings retain their sources; research and simulation are the next layers.

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A reference for what the literature reports. Not medical advice.

© 2026 CatalystPrivacy TermsReference data under the licences listed on the attribution page.

Index

Diseases

Names from Mondo, HPO and GenCC

diseases in the graph: 23,730

Filter diseases by name

#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

20,601–20,700 of 23,730, alphabetically

sialolithiasisMondoMONDO:0006970
sialuriaMondoMONDO:0010028
Siberian tick typhusMondoMONDO:0001154
sick building syndromeMondoMONDO:0005959
sick sinus syndromeMondoMONDO:0001823
sick sinus syndrome 1Mondo

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

MONDO:0024562

sick sinus syndrome 2, autosomal dominantMondoMONDO:0008102

sick sinus syndrome 3, susceptibility toMondoMONDO:0013568

sick sinus syndrome 4MondoMONDO:0859173

sickle cell diseaseMondoMONDO:0011382

sickle cell disease due to hemoglobin S and a non-S/non-C hemoglobin variantMondoMONDO:0979354

sickle cell S-Lepore diseaseMondoMONDO:0981004

sickle cell S-O Arab diseaseMondoMONDO:0981005

sickle cell-beta plus-thalassemiaMondoMONDO:0979287

sickle cell-beta zero-thalassemiaMondoMONDO:0979286

sickle cell-beta-thalassemia disease syndromeMondoMONDO:0016668

sickle cell-hemoglobin c disease syndromeMondoMONDO:0016669

sickle cell-hemoglobin d disease syndromeMondoMONDO:0016670

sickle cell-hemoglobin E disease syndromeMondoMONDO:0016671

Siddiqi syndromeMondoMONDO:0032842

sideroblastic anemiaMondoMONDO:0015194

sideroblastic anemia 2MondoMONDO:0008785

sideroblastic anemia 3MondoMONDO:0014804

Siegler-Brewer-Carey syndromeMondoMONDO:0017849

Sifrim-Hitz-Weiss syndromeMondoMONDO:0014946

sigmoid colon cancerMondoMONDO:0001464

sigmoid diseaseMondoMONDO:0002139

sigmoid neoplasmMondoMONDO:0006971

signet ring basal cell carcinomaMondoMONDO:0002958

signet ring cell breast carcinomaMondoMONDO:0002671

signet ring cell carcinomaMondoMONDO:0005092

signet ring cell gastric adenocarcinomaMondoMONDO:0006409

signet ring cell intrahepatic cholangiocarcinomaMondoMONDO:0004346

signet ring cell variant cervical mucinous adenocarcinomaMondoMONDO:0003768

silent myocardial infarctionMondoMONDO:0003678

silent pituitary adenomaMondoMONDO:0017825

silent sinus syndromeMondoMONDO:0019108

silicosiderosisMondoMONDO:0043283

silicosisMondoMONDO:0005960

silicotuberculosisMondoMONDO:0021804

Sillence syndromeMondoMONDO:0007227

silo filler diseaseMondoMONDO:0006972

Silver-Russell syndromeMondoMONDO:0008394

Silver-Russell syndrome 1MondoMONDO:0020796

silver-russell syndrome 2MondoMONDO:0030116

Silver-Russell syndrome 3MondoMONDO:0014663

silver-russell syndrome 4MondoMONDO:0030118

Silver-Russell syndrome 5MondoMONDO:0020795

silver-Russell syndrome due to 11p15 microduplicationMondoMONDO:0016481

silver-Russell syndrome due to 7p11.2p13 microduplicationMondoMONDO:0016479

silver-Russell syndrome due to an imprinting defect of 11p15MondoMONDO:0016480

silver-Russell syndrome due to maternal uniparental disomy of chromosome 11MondoMONDO:0016482

silver-Russell syndrome due to maternal uniparental disomy of chromosome 7MondoMONDO:0019913

Silverman-Handmaker type dyssegmental dysplasiaMondoMONDO:0009140

SIM1-related Prader-Willi-like syndromeMondoMONDO:0018355

simple chronic conjunctivitisMondoMONDO:0004811

simple cryoglobulinemiaMondoMONDO:0019606

simple endometrial hyperplasiaMondoMONDO:0006410

simple partial epilepsyMondoMONDO:0003290

Simpson-Golabi-Behmel syndromeMondoMONDO:0010731

Simpson-Golabi-Behmel syndrome type 1MondoMONDO:0020602

Simpson-Golabi-Behmel syndrome type 2MondoMONDO:0010265

simultanagnosiaMondoMONDO:0000678

SIN3A-related intellectual disability syndromeMondoMONDO:0044699

SIN3A-related intellectual disability syndrome due to a point mutationMondoMONDO:0044700

Sinding-Larsen-Johansson diseaseMondoMONDO:0019970

single isolated optic neuritisMondoMONDO:0971049

single-organ polyarteritis nodosaMondoMONDO:0018595

single-system multifocal langerhans cell histiocytosisMondoMONDO:0975908

Singleton-Merten dysplasiaMondoMONDO:0008429

Singleton-Merten syndrome 1MondoMONDO:0024535

Singleton-Merten syndrome 2MondoMONDO:0014575

sino-auricular heart blockMondoMONDO:0015257

sinoatrial blockMondoMONDO:0020806

sinoatrial node disorderMondoMONDO:0000469

sinoatrial node dysfunction and deafnessMondoMONDO:0013960

sinonasal undifferentiated carcinomaMondoMONDO:0006411

sinus histiocytosis with massive lymphadenopathyMondoMONDO:0006412

sinus node disease and myopiaMondoMONDO:0008423

sinusitisMondoMONDO:0005961

sirenomeliaMondoMONDO:0017850

sister chromatid exchange, frequency ofMondoMONDO:0008427

sitosterolemiaMondoMONDO:0008863

sitosterolemia 1MondoMONDO:0020747

sitosterolemia 2MondoMONDO:0020748

situs inversusMondoMONDO:0010029

situs inversus totalis with cystic dysplasia of kidneys and pancreasMondoMONDO:0011354

six2-related frontonasal dysplasiaMondoMONDO:0044628

Sjogren syndromeMondoMONDO:0010030

Sjogren-Larsson syndromeMondoMONDO:0010031

Sjogren-Larsson-like ichthyosis without CNS or eye involvementMondoMONDO:0010032

skeletal defects, genital hypoplasia, and intellectual disabilityMondoMONDO:0012909

skeletal dysplasiaMondoMONDO:0018230

skeletal dysplasia and progressive central nervous system degeneration, lethalMondoMONDO:0011263

skeletal dysplasia with delayed epiphyseal and carpal bone ossificationMondoMONDO:0008430

skeletal dysplasia-epilepsy-short stature syndromeMondoMONDO:0011011

skeletal dysplasia-intellectual disability syndromeMondoMONDO:0010668

skeletal dysplasia-T-cell immunodeficiency-developmental delay syndromeMondoMONDO:0033682

skeletal dysplasia, mild, with joint laxity and advanced bone ageMondoMONDO:0030029

skeletal dysplasia, rhizomelic, with retinitis pigmentosaMondoMONDO:0012182

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