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Evidence

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

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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

674 of 23,730 begin with R

RAB18 deficiencyMondoMONDO:0700247
RAB23-related Carpenter syndromeMondoMONDO:0008710
RAB28-related retinopathyMondoMONDO:0100448
rabiesMondoMONDO:0019173
Rabin-Pappas syndromeMondoMONDO:0859331
Rabson-Mendenhall syndromeMondo

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

MONDO:0009874

RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndromeMondoMONDO:0979261

RAD51C-related cancer predispositionMondoMONDO:0700273

RAD51D-related cancer predispositionMondoMONDO:0700274

radial defect robin sequenceMondoMONDO:0043191

radial deficiency-tibial hypoplasia syndromeMondoMONDO:0015232

radial heads, posterior dislocation ofMondoMONDO:0008356

radial hemimeliaMondoMONDO:0019671

radial hemimelia, bilateralMondoMONDO:0017487

radial hemimelia, unilateralMondoMONDO:0017486

radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndromeMondoMONDO:0008357

radial nerve lesionMondoMONDO:0006940

radial neuropathyMondoMONDO:0001459

radial ray deficiency, X-linkedMondoMONDO:0010312

radial ray hypoplasia-choanal atresia syndromeMondoMONDO:0008358

radiation cystitisMondoMONDO:0004112

radiation myelitisMondoMONDO:0019529

radiation pneumonitisMondoMONDO:0043919

radiation proctitisMondoMONDO:0019084

radiation sensitivity of natural killer activityMondoMONDO:0010719

radiation sensitivity/chromosome instability syndrome, autosomal dominantMondoMONDO:0011557

radiation-induced disorderMondoMONDO:0043459

radiation-induced meningiomaMondoMONDO:0011648

radiation-induced neuropathyMondoMONDO:0100635

radiation-induced plexopathyMondoMONDO:0033838

radiculitisMondoMONDO:0021765

radiculoneuropathy, fatal neonatalMondoMONDO:0009951

radiculopathyMondoMONDO:0002959

radio-digito-facial dysplasiaMondoMONDO:0024171

radio-renal syndromeMondoMONDO:0008359

Radio-Tartaglia syndromeMondoMONDO:0859143

radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndromeMondoMONDO:0011555

radio-ulnar synostosis, bilateralMondoMONDO:0017555

radio-ulnar synostosis, unilateralMondoMONDO:0017554

radiodermatitisMondoMONDO:0043771

radioulnar synostosis with amegakaryocytic thrombocytopenia 1MondoMONDO:0024558

radioulnar synostosis with amegakaryocytic thrombocytopenia 2MondoMONDO:0014758

radioulnar synostosis-developmental delay-hypotonia syndromeMondoMONDO:0009952

radioulnar synostosis-microcephaly-scoliosis syndromeMondoMONDO:0011320

radioulnar synostosis, nonsyndromic, susceptibility toMondoMONDO:0100183

radioulnar synostosis, radial ray abnormalities, and severe malformations in the maleMondoMONDO:0010276

radius, aplasia of, with cleft lip/palateMondoMONDO:0008361

Rafiq syndromeMondoMONDO:0013624

ragopathyMondoMONDO:0976294

ragweed sensitivityMondoMONDO:0008362

Rahman syndromeMondoMONDO:0044323

raindrop hypopigmentationMondoMONDO:0008363

Rajab interstitial lung disease with brain calcificationsMondoMONDO:0100214

Rajab interstitial lung disease with brain calcifications 1MondoMONDO:0100215

Rajab interstitial lung disease with brain calcifications 2MondoMONDO:0100220

raltegravir toxicityMondoMONDO:0027687

Ramon syndromeMondoMONDO:0009954

Ramond-Elliott neurodevelopmental syndromeMondoMONDO:0980751

Ramos-Arroyo syndromeMondoMONDO:0007382

rapadilino syndromeMondoMONDO:0009955

rapid eye movement sleep disorderMondoMONDO:0024363

rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndromeMondoMONDO:0017408

rapidly involuting congenital hemangiomaMondoMONDO:0015404

rapidly progressive glomerulonephritisMondoMONDO:0017236

rapidly progressive primary central nervous system vasculitisMondoMONDO:0100248

Rapp-Hodgkin syndromeMondoMONDO:0007508

Rasmussen subacute encephalitisMondoMONDO:0016019

RASopathyMondoMONDO:0021060

rat-bite feverMondoMONDO:0006941

Rauch-Steindl syndromeMondoMONDO:0859219

ravine syndromeMondoMONDO:0020505

Raynaud diseaseMondoMONDO:0008364

RBFOX2-related congenital heart disorderMondoMONDO:0100557

RCBTB1-related retinopathyMondoMONDO:0014955

RD3-related retinopathyMondoMONDO:0700235

RDH12-related dominant retinopathyMondoMONDO:0800100

RDH12-related recessive retinopathyMondoMONDO:0800099

RDH5-related retinopathyMondoMONDO:0100443

reactive airway diseaseMondoMONDO:0100470

reactive angioendotheliomatosisMondoMONDO:0975756

reactive arthritisMondoMONDO:0017376

reactive cutaneous fibrous lesionMondoMONDO:0006603

reactive thrombocytosisMondoMONDO:0024518

reading disorderMondoMONDO:0001697

reading seizuresMondoMONDO:0007560

recessive aplasia cutis congenita of limbsMondoMONDO:0010876

recessive dystrophic epidermolysis bullosaMondoMONDO:0009179

recessive dystrophic epidermolysis bullosa inversaMondoMONDO:0019310

recessive dystrophic epidermolysis bullosa-generalized otherMondoMONDO:0019522

recessive intellectual disability-motor dysfunction-multiple joint contractures syndromeMondoMONDO:0017232

recessive mitochondrial ataxia syndromeMondoMONDO:0019791

recessive X-linked ichthyosisMondoMONDO:0010622

reciprocal translocation down syndromeMondoMONDO:0700083

recombinant 8 syndromeMondoMONDO:0008365

recombinase activating gene 1 deficiencyMondoMONDO:0000572

recombinase activating gene 2 deficiencyMondoMONDO:0000573

RECON progeroid syndromeMondoMONDO:0957266

rectal adenosquamous carcinomaMondoMONDO:0056817

rectal cancerMondoMONDO:0006519

rectal carcinomaMondoMONDO:0044937

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