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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

7,101–7,200 of 23,730, alphabetically

digestive system neuroendocrine neoplasmMondoMONDO:0024503
digestive system neuroendocrine tumor, grade 1/2MondoMONDO:0000386
digital anomalies-intellectual disability-short stature syndromeMondoMONDO:0018122
digital papillary eccrine carcinomaMondoMONDO:0044789
digitalis poisoningMondoMONDO:0017863

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

digitotalar dysmorphism

MondoMONDO:0015240

digitotalar dysmorphism; ulnar drift, hereditaryMondoMONDO:0007458

dihydropteridine reductase deficiencyMondoMONDO:0009862

dihydropyrimidine dehydrogenase deficiencyMondoMONDO:0010130

dihydropyrimidinuriaMondoMONDO:0009111

dilated cardiomyopathyMondoMONDO:0005021

dilated cardiomyopathy 1AMondoMONDO:0007269

dilated cardiomyopathy 1AAMondoMONDO:0012808

dilated cardiomyopathy 1BMondoMONDO:0010951

dilated cardiomyopathy 1BBMondoMONDO:0013030

dilated cardiomyopathy 1CMondoMONDO:0011094

dilated cardiomyopathy 1CCMondoMONDO:0013147

dilated cardiomyopathy 1DMondoMONDO:0011095

dilated cardiomyopathy 1DDMondoMONDO:0013168

dilated cardiomyopathy 1EMondoMONDO:0011003

dilated cardiomyopathy 1EEMondoMONDO:0013198

dilated cardiomyopathy 1FFMondoMONDO:0013211

dilated cardiomyopathy 1GMondoMONDO:0011400

dilated cardiomyopathy 1GGMondoMONDO:0013339

dilated cardiomyopathy 1HMondoMONDO:0011425

dilated cardiomyopathy 1HHMondoMONDO:0013479

dilated cardiomyopathy 1IMondoMONDO:0011482

dilated cardiomyopathy 1IIMondoMONDO:0014073

dilated cardiomyopathy 1JMondoMONDO:0011541

dilated cardiomyopathy 1JJMondoMONDO:0014095

dilated cardiomyopathy 1KMondoMONDO:0011567

dilated cardiomyopathy 1KKMondoMONDO:0014100

dilated cardiomyopathy 1LMondoMONDO:0011702

dilated cardiomyopathy 1MMondoMONDO:0011840

dilated cardiomyopathy 1NNMondoMONDO:0014396

dilated cardiomyopathy 1OMondoMONDO:0012062

dilated cardiomyopathy 1PMondoMONDO:0012362

dilated cardiomyopathy 1QMondoMONDO:0012364

dilated cardiomyopathy 1RMondoMONDO:0013261

dilated cardiomyopathy 1SMondoMONDO:0013262

dilated cardiomyopathy 1UMondoMONDO:0013371

dilated cardiomyopathy 1VMondoMONDO:0013373

dilated cardiomyopathy 1WMondoMONDO:0012667

dilated cardiomyopathy 1XMondoMONDO:0012704

dilated cardiomyopathy 1YMondoMONDO:0012744

dilated cardiomyopathy 1ZMondoMONDO:0012745

dilated cardiomyopathy 2AMondoMONDO:0012746

dilated cardiomyopathy 2BMondoMONDO:0013848

dilated cardiomyopathy 3BMondoMONDO:0010542

dilated cardiomyopathy-hypergonadotropic hypogonadism syndromeMondoMONDO:0008915

dilution, pigmentaryMondoMONDO:0007459

dimethylglycine dehydrogenase deficiencyMondoMONDO:0011610

dioctophymiasisMondoMONDO:0000298

diomedi bernardi placidi syndromeMondoMONDO:0022989

DIP2C-related developmental disorder with speech delayMondoMONDO:0700356

diphalliaMondoMONDO:0016416

diphallus rachischisis imperforate anusMondoMONDO:0022990

diphtheriaMondoMONDO:0005504

diphtheritic cystitisMondoMONDO:0001681

diphtheritic myocarditisMondoMONDO:0041259

diphtheritic peritonitisMondoMONDO:0001682

diphyllobothriasisMondoMONDO:0015260

diplegia of upper limbMondoMONDO:0004618

diploid-triploid mosaicismMondoMONDO:0022991

diprosopusMondoMONDO:0015672

dipsogenic diabetes insipidusMondoMONDO:0022993

dirofilariasisMondoMONDO:0015636

disabling pansclerotic morphea of childhoodMondoMONDO:0957497

disappearing bone diseaseMondoMONDO:0003157

discharging earMondoMONDO:0000988

discoid lupus erythematosusMondoMONDO:0019558

discoid lupus erythematosus of eyelidMondoMONDO:0004706

discrete fibromuscular subaortic stenosisMondoMONDO:0020393

discrete papular lichen myxedematosusMondoMONDO:0019579

discrete subaortic stenosisMondoMONDO:0006729

discrimination, Two-point, reduction 1NMondoMONDO:0007460

disease arising from reactivation of latent virusMondoMONDO:0100330

disease by body system or componentMondoMONDO:7770006

disease by developmental or physiological processMondoMONDO:7770007

disease by etiologic mechanismMondoMONDO:7770008

disease by molecular mechanismMondoMONDO:7770011

disease of bone structureMondoMONDO:0000836

disease of genetic or genomic mechanismMondoMONDO:7770009

disease of orbital part of eye adnexaMondoMONDO:0004751

disease of primarily extrinsic mechanismMondoMONDO:7770010

disease of the tendonMondoMONDO:0100010

disease related to hematopoietic stem cell transplantMondoMONDO:0700222

disease related to solid organ transplantationMondoMONDO:0700221

disease related to transplantationMondoMONDO:0700220

disease susceptibilityMondoMONDO:0042489

dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disabilityMondoMONDO:0011290

dislocation of ear ossicleMondoMONDO:0001199

dislocation of the hip-dysmorphism syndromeMondoMONDO:0011081

disorder of acid-base balanceMondoMONDO:0041261

disorder of appendixMondoMONDO:0056798

disorder of beta and omega amino acid metabolismMondoMONDO:0017684

disorder of bile acid aminotransferaseMondoMONDO:0100304

disorder of carbohydrate transmembrane transport and absorptionMondoMONDO:0017706

disorder of carnitine cycle and carnitine transportMondoMONDO:0017716

disorder of catecholamine synthesisMondoMONDO:0017759

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