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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

1,601–1,700 of 23,730, alphabetically

apical myocardial infarctionMondoMONDO:0003673
aplasia cutis autosomal recessiveMondoMONDO:0021907
aplasia cutis congenitaMondoMONDO:0007145
aplasia cutis congenita dominantMondoMONDO:0021908
aplasia cutis congenita-intestinal lymphangiectasia syndromeMondoMONDO:0008808

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

aplasia cutis-enamel dysplasia syndrome

MondoMONDO:0968978

aplasia cutis-myopia syndromeMondoMONDO:0010988

aplasia of lacrimal and salivary glandsMondoMONDO:0008397

aplastic anemiaMondoMONDO:0015909

aplastic anemia, susceptibility toMondoMONDO:0800414

apnea of prematurityMondoMONDO:0020567

APO A-i deficiencyMondoMONDO:0022481

apocrine adenocarcinomaMondoMONDO:0003214

apocrine adenomaMondoMONDO:0002804

apocrine adenosis of breastMondoMONDO:0003726

apocrine sweat gland cancerMondoMONDO:0003215

apocrine sweat gland disorderMondoMONDO:0024467

apocrine sweat gland neoplasmMondoMONDO:0003686

apodiaMondoMONDO:0017446

apodia, bilateralMondoMONDO:0017505

apodia, unilateralMondoMONDO:0017504

apolipoprotein A-I deficiencyMondoMONDO:0700513

apolipoprotein A-II amyloidosisMondoMONDO:0016533

apolipoprotein A-II deficiencyMondoMONDO:0980749

apolipoprotein c-III deficiencyMondoMONDO:0013534

APP-related brain and vascular amyloidosisMondoMONDO:1060190

apparent mineralocorticoid excessMondoMONDO:0009025

appendiceal neoplasmMondoMONDO:0001236

appendicitisMondoMONDO:0005649

appendicitis, proneness toMondoMONDO:0007148

appendix adenocarcinomaMondoMONDO:0006087

appendix adenomaMondoMONDO:0006088

appendix cancerMondoMONDO:0001235

appendix carcinomaMondoMONDO:0003196

appendix hyperplastic polypMondoMONDO:0006090

appendix L-cell glucagon-like peptide-producing neuroendocrine tumorMondoMONDO:0021101

appendix leiomyomaMondoMONDO:0003300

appendix lymphomaMondoMONDO:0001237

appendix mucinous cystadenocarcinomaMondoMONDO:0002703

appendix neuroendocrine neoplasmMondoMONDO:0024501

appendix neuroendocrine tumor G1MondoMONDO:0006091

appendix villous adenomaMondoMONDO:0006092

apperceptive agnosiaMondoMONDO:0000664

apraxiaMondoMONDO:0000665

apraxia of eyelid openingMondoMONDO:0011289

aprosencephalyMondoMONDO:0035450

aprosencephaly cerebellar dysgenesisMondoMONDO:0011062

aquagenic palmoplantar keratodermaMondoMONDO:0044663

aquagenic pruritusMondoMONDO:0021913

aquarium granulomaMondoMONDO:0043314

aqueous misdirectionMondoMONDO:0001206

arachnodactyly-abnormal ossification-intellectual disability syndromeMondoMONDO:0015234

arachnodactyly-intellectual disability-dysmorphism syndromeMondoMONDO:0015235

arachnoid cystMondoMONDO:0008813

arachnoiditisMondoMONDO:0015304

arakawa syndrome 2MondoMONDO:0021915

arbovirus feverMondoMONDO:0018093

arbovirus infectionMondoMONDO:0020731

arcus senilisMondoMONDO:0007150

AREDYLD syndromeMondoMONDO:0008812

aregenerative anemiaMondoMONDO:0015100

arena syndromeMondoMONDO:0021918

Arenaviridae infectious diseaseMondoMONDO:0005650

arenavirus hemorrhagic feverMondoMONDO:0005651

ARF3-related neurodevelopmental disorderMondoMONDO:0700366

Argentine hemorrhagic feverMondoMONDO:0017874

arginase deficiencyMondoMONDO:0008814

argininosuccinic aciduriaMondoMONDO:0008815

Argyll Robertson pupilMondoMONDO:0001986

argyriaMondoMONDO:0018952

argyrophilic grain diseaseMondoMONDO:0700351

ARHGAP29-related non-syndromic orofacial cleftMondoMONDO:1060132

arhinia, choanal atresia, and microphthalmiaMondoMONDO:0011323

ariboflavinosisMondoMONDO:0004573

ARL6-related ciliopathyMondoMONDO:1040065

Armfield syndromeMondoMONDO:0010284

arms, malformation ofMondoMONDO:0007151

Arnold stickler bourne syndromeMondoMONDO:0021921

aromatase deficiencyMondoMONDO:0013301

aromatase excess syndromeMondoMONDO:0007690

aromatic L-amino acid decarboxylase deficiencyMondoMONDO:0012084

arrhiniaMondoMONDO:0015237

arrhythmogenic cardiomyopathy with variable ectodermal abnormalitiesMondoMONDO:0957795

arrhythmogenic cardiomyopathy with wooly hair and keratodermaMondoMONDO:0011581

arrhythmogenic right ventricular cardiomyopathyMondoMONDO:0016587

arrhythmogenic right ventricular dysplasia 1MondoMONDO:0007152

arrhythmogenic right ventricular dysplasia 10MondoMONDO:0012434

arrhythmogenic right ventricular dysplasia 11MondoMONDO:0012506

arrhythmogenic right ventricular dysplasia 12MondoMONDO:0012684

arrhythmogenic right ventricular dysplasia 13MondoMONDO:0000908

arrhythmogenic right ventricular dysplasia 3MondoMONDO:0011188

arrhythmogenic right ventricular dysplasia 4MondoMONDO:0011189

arrhythmogenic right ventricular dysplasia 5MondoMONDO:0011459

arrhythmogenic right ventricular dysplasia 6MondoMONDO:0011460

arrhythmogenic right ventricular dysplasia 8MondoMONDO:0011831

arrhythmogenic right ventricular dysplasia 9MondoMONDO:0012180

arrhythmogenic right ventricular dysplasia, familial, 14MondoMONDO:0030062

Arroyo Garcia Cimadevilla syndromeMondoMONDO:0021923

arterial calcification of infancyMondoMONDO:0018870

arterial calcification, generalized, of infancy, 1MondoMONDO:0008817

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