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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

10,101–10,200 of 23,730, alphabetically

hemidystoniaMondoMONDO:0000487
hemidystonia-hemiatrophy syndromeMondoMONDO:0017649
hemifacial hypertrophyMondoMONDO:0007590
hemifacial myohyperplasiaMondoMONDO:0011723
hemihydranencephalyMondoMONDO:1040007
hemihyperplasia-multiple lipomatosis syndrome

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

MondoMONDO:0017177

hemimegalencephalyMondoMONDO:0020492

hemimeliaMondoMONDO:0016240

hemiparkinsonism-hemiatrophy syndromeMondoMONDO:0017636

hemiplegiaMondoMONDO:0001170

hemiplegic migraine-developmental and epileptic encephalopathy spectrumMondoMONDO:0100539

hemochromatosis type 1MondoMONDO:0021001

hemochromatosis type 2MondoMONDO:0019257

hemochromatosis type 2AMondoMONDO:0011216

hemochromatosis type 2BMondoMONDO:0013220

hemochromatosis type 3MondoMONDO:0011417

hemochromatosis type 4MondoMONDO:0011631

hemochromatosis type 5MondoMONDO:0014225

hemoglobin C diseaseMondoMONDO:0016242

hemoglobin C-beta-thalassemia syndromeMondoMONDO:0016490

hemoglobin D diseaseMondoMONDO:0019537

hemoglobin E diseaseMondoMONDO:0016243

hemoglobin E-beta-thalassemia syndromeMondoMONDO:0016491

hemoglobin H diseaseMondoMONDO:0013512

hemoglobin Lepore-beta-thalassemia syndromeMondoMONDO:0018022

hemoglobin M diseaseMondoMONDO:0018023

hemoglobin--variants for which the chain carrying the mutation 1S unknown or uncertainMondoMONDO:0007717

hemoglobinopathyMondoMONDO:0044348

hemoglobinopathy Toms RiverMondoMONDO:0017238

hemoglobinuriaMondoMONDO:0003656

hemolytic anemiaMondoMONDO:0003664

hemolytic anemia due to adenylate kinase deficiencyMondoMONDO:0012967

hemolytic anemia due to diphosphoglycerate mutase deficiencyMondoMONDO:0009113

hemolytic anemia due to erythrocyte adenosine deaminase overproductionMondoMONDO:0020458

hemolytic anemia due to glucophosphate isomerase deficiencyMondoMONDO:0013275

hemolytic anemia due to glutathione reductase deficiencyMondoMONDO:0019531

hemolytic anemia due to pyrimidine 5' nucleotidase deficiencyMondoMONDO:0009946

hemolytic anemia with thermal sensitivity of red cellsMondoMONDO:0009334

hemolytic disease of fetus and newborn, RH-inducedMondoMONDO:0859172

hemolytic disease of the newborn with Kell alloimmunizationMondoMONDO:0017164

hemolytic poikilocytic anemia due to reduced ankyrin binding sitesMondoMONDO:0007715

hemolytic uremic syndrome, atypical, 8, with rhizomelic short statureMondoMONDO:0957495

hemolytic uremic syndrome, atypical, susceptibility to, 1MondoMONDO:0009335

hemolytic uremic syndrome, atypical, susceptibility to, 7MondoMONDO:0100590

hemolytic-uremic syndromeMondoMONDO:0001549

hemometraMondoMONDO:0006782

hemopericardiumMondoMONDO:0005783

hemophagocytic lymphohistiocytosis due to RhoG deficiencyMondoMONDO:0800147

hemophagocytic lymphohistiocytosis, familial, 6MondoMONDO:0033557

hemophagocytic syndromeMondoMONDO:0015540

hemophiliaMondoMONDO:0018660

hemophilia AMondoMONDO:0010602

hemophilia A with vascular abnormalityMondoMONDO:0010603

hemophilia BMondoMONDO:0010604

hemophilia B leydenMondoMONDO:0850054

hemophilic arthropathyMondoMONDO:0043240

hemopneumothoraxMondoMONDO:0006783

hemopoietic proliferationMondoMONDO:0010605

hemorrhage, intracerebral, susceptibility toMondoMONDO:0100533

hemorrhagic cystitisMondoMONDO:0000496

hemorrhagic diseaseMondoMONDO:0002243

hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutationMondoMONDO:0015801

hemorrhagic disease of newbornMondoMONDO:0006784

hemorrhagic duodenitisMondoMONDO:0024415

hemorrhagic feverMondoMONDO:0600002

hemorrhagic fever-renal syndromeMondoMONDO:0018081

hemorrhagic strokeMondoMONDO:1060199

hemorrhoidMondoMONDO:0004872

hemosiderosisMondoMONDO:0001436

hemosiderosis, pulmonary, with deficiency of gamma-a globulinMondoMONDO:0009336

Hendra virus infectionMondoMONDO:0017942

Hengel-Maroofian-Schols syndromeMondoMONDO:0859208

henipavirus infectious diseaseMondoMONDO:0005785

Hennekam lymphangiectasia-lymphedema syndrome 1MondoMONDO:0009337

Hennekam lymphangiectasia-lymphedema syndrome 2MondoMONDO:0014454

hennekam lymphangiectasia-lymphedema syndrome 3MondoMONDO:0032564

Hennekam syndromeMondoMONDO:0016256

Hennekam-Beemer syndromeMondoMONDO:0009569

Hepadnaviridae infectious diseaseMondoMONDO:0005786

heparin cofactor 2 deficiencyMondoMONDO:0012876

heparin-induced thrombocytopeniaMondoMONDO:0018048

hepatic adenomas, familialMondoMONDO:0007718

hepatic angiomyolipomaMondoMONDO:0002605

hepatic comaMondoMONDO:0001548

hepatic cutaneous porphyriaMondoMONDO:0971154

hepatic encephalopathyMondoMONDO:0001711

hepatic fibrinogen storage diseaseMondoMONDO:7770747

hepatic fibrosis-renal cysts-intellectual disability syndromeMondoMONDO:0008941

hepatic fibrosis, severe, susceptibility to, due to Schistosoma mansoni infectionMondoMONDO:0011409

hepatic flexure cancerMondoMONDO:0002357

hepatic granulomaMondoMONDO:0006241

hepatic infarctionMondoMONDO:0001787

hepatic porphyriaMondoMONDO:0002520

hepatic tuberculosisMondoMONDO:0005787

hepatic vascular disorderMondoMONDO:0002405

hepatic vein thrombosisMondoMONDO:0006786

hepatic veno-occlusive diseaseMondoMONDO:0019514

hepatic veno-occlusive disease-immunodeficiency syndromeMondoMONDO:0009338

hepatitisMondoMONDO:0002251

hepatitis A virus infectionMondoMONDO:0005790

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