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Evidence

CompoundsSubstances with curated findings
OutcomesMeasured endpoints
ProteinsTransporters and enzymes
InteractionsPairs that share biology
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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

7,601–7,700 of 23,730, alphabetically

ear antitragus, tag at base ofMondoMONDO:0007497
ear exostosesMondoMONDO:0007498
ear foldingMondoMONDO:0007499
ear infectionMondoMONDO:0021666
ear malformationMondoMONDO:0007500
ear neoplasmMondoMONDO:0021233

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

ear pits, posterior helicalMondoMONDO:0007502

ear without helixMondoMONDO:0007503

early congenital syphilisMondoMONDO:0000333

early invasive cervical adenocarcinomaMondoMONDO:0004530

early onset hypertensionMondoMONDO:0005430

early repolarization associated with ventricular fibrillationMondoMONDO:0013318

early response to neural induction geneMondoMONDO:0011516

early T cell progenitor acute lymphoblastic leukemiaMondoMONDO:0100291

early yawsMondoMONDO:0001067

early-childhood-onset neurodegeneration with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathyMondoMONDO:0700288

early-infantile DEEMondoMONDO:0800491

early-onset anterior polar cataractMondoMONDO:0020373

early-onset autoimmune disorder due to DOCK11 partial deficiencyMondoMONDO:0958137

early-onset autoimmunity-autoinflammation-immunodeficiency syndromeMondoMONDO:0850068

early-onset autosomal dominant Alzheimer diseaseMondoMONDO:0015140

early-onset calcifying leukoencephalopathy-skeletal dysplasiaMondoMONDO:0034143

early-onset cerebellar ataxia with retained tendon reflexesMondoMONDO:0008938

early-onset combined immunodeficiency with low ig due to dominant negative IKAROS mutationMondoMONDO:0979316

early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutationMondoMONDO:0017325

early-onset familial hypoaldosteronismMondoMONDO:0035320

early-onset familial noncirrhotic portal hypertensionMondoMONDO:0044631

early-onset generalized dystoniaMondoMONDO:0100016

early-onset generalized limb-onset dystoniaMondoMONDO:0007492

early-onset idiopathic chronic pancreatitisMondoMONDO:0981007

early-onset immune dysregulation due to DOCK11 complete deficiencyMondoMONDO:0958138

early-onset Lafora body diseaseMondoMONDO:0014717

early-onset lamellar cataractMondoMONDO:0018611

early-onset myopathy with fatal cardiomyopathyMondoMONDO:0012714

early-onset non-syndromic cataractMondoMONDO:0011060

early-onset nuclear cataractMondoMONDO:0020376

early-onset obesity-hyperphagia-severe developmental delay syndromeMondoMONDO:0850115

early-onset Parkinson disease 20MondoMONDO:0014233

early-onset parkinsonism-intellectual disability syndromeMondoMONDO:0010709

early-onset partial cataractMondoMONDO:0020377

early-onset posterior polar cataractMondoMONDO:0020378

early-onset posterior subcapsular cataractMondoMONDO:0018610

early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndromeMondoMONDO:0044646

early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndromeMondoMONDO:0044696

early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndromeMondoMONDO:0044651

early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndromeMondoMONDO:0014209

early-onset pulmonary and cutaneous vasculitisMondoMONDO:0800137

early-onset schizophreniaMondoMONDO:0019939

early-onset sutural cataractMondoMONDO:0020372

early-onset zonular cataractMondoMONDO:0020379

EAST syndromeMondoMONDO:0013005

East Texas bleeding disorderMondoMONDO:0011615

eastern equine encephalitisMondoMONDO:0005736

eating disorderMondoMONDO:0005451

eating seizuresMondoMONDO:0015645

Ebola hemorrhagic feverMondoMONDO:0005737

Ebstein anomalyMondoMONDO:0009144

Ebstein-Bezieau neurodevelopmental syndromeMondoMONDO:0981163

EBV-positive T-cell lymphoproliferative disorder of childhoodMondoMONDO:0006188

eccrine acrospiromaMondoMONDO:0006738

eccrine angiomatous hamartomaMondoMONDO:0975755

eccrine carcinomaMondoMONDO:0024240

eccrine mixed tumor of skinMondoMONDO:0002200

eccrine mucinous carcinomaMondoMONDO:0023039

eccrine papillary adenomaMondoMONDO:0003450

eccrine porocarcinomaMondoMONDO:0006189

eccrine sweat gland cancerMondoMONDO:0005506

eccrine sweat gland hamartomaMondoMONDO:0024482

eccrine sweat gland neoplasmMondoMONDO:0002090

eccrine syringofibroadenomatosis with eyelid abnormalitiesMondoMONDO:0011357

echinococcosisMondoMONDO:0005738

echinococcus granulosus infectious diseaseMondoMONDO:0044346

echinostomiasisMondoMONDO:0005739

echolaliaMondoMONDO:0002904

Echovirus infectious diseaseMondoMONDO:0005740

ECHS1-related paroxysmal dyskinesiaMondoMONDO:0100019

eclampsiaMondoMONDO:0001754

ectasia of the left appendageMondoMONDO:0020433

ectasia of the right atrial appendageMondoMONDO:0020432

ecthymaMondoMONDO:0001404

ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominantMondoMONDO:0007509

ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessiveMondoMONDO:0009147

ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominantMondoMONDO:0013982

ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessiveMondoMONDO:0013983

ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail typeMondoMONDO:0015024

ectodermal dysplasia 13, hair/tooth typeMondoMONDO:0044305

ectodermal dysplasia 14, hair/tooth type with or without hypohidrosisMondoMONDO:0032584

ectodermal dysplasia 15, hypohidrotic/hair typeMondoMONDO:0032804

ectodermal dysplasia 17 with or without limb malformationsMondoMONDO:0979228

ectodermal dysplasia 4, hair/nail typeMondoMONDO:0011177

ectodermal dysplasia 5, hair/nail typeMondoMONDO:0013973

ectodermal dysplasia 6, hair/nail typeMondoMONDO:0013974

ectodermal dysplasia 7, hair/nail typeMondoMONDO:0013975

ectodermal dysplasia 9, hair/nail typeMondoMONDO:0013976

ectodermal dysplasia alopecia preaxial polydactylyMondoMONDO:0023043

ectodermal dysplasia and immune deficiencyMondoMONDO:0010293

ectodermal dysplasia and immunodeficiency 1MondoMONDO:0020740

ectodermal dysplasia and immunodeficiency 2MondoMONDO:0012806

ectodermal dysplasia arthrogryposis diabetes mellitusMondoMONDO:0023045

ectodermal dysplasia Bartalos typeMondoMONDO:0023040

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