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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

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

840 of 23,730 begin with L

laryngo-onycho-cutaneous syndromeMondoMONDO:0009513
laryngoceleMondoMONDO:0016530
laryngospasm, severe neonatal episodicMondoMONDO:0800339
laryngostenosisMondoMONDO:0001305
laryngotracheal angiomaMondoMONDO:0015317
laryngotracheitisMondo

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

MONDO:0000263

laryngotracheoesophageal cleftMondoMONDO:0016060

laryngotracheoesophageal cleft type 0MondoMONDO:0017220

laryngotracheoesophageal cleft type 1MondoMONDO:0019761

laryngotracheoesophageal cleft type 2MondoMONDO:0019762

laryngotracheoesophageal cleft type 3MondoMONDO:0019763

laryngotracheoesophageal cleft type 4MondoMONDO:0019764

larynx atresiaMondoMONDO:0007879

larynx cancerMondoMONDO:0002352

larynx carcinoma in situMondoMONDO:0004696

larynx liposarcomaMondoMONDO:0003588

larynx squamous papillomaMondoMONDO:0000935

larynx verrucous carcinomaMondoMONDO:0002766

Lassa feverMondoMONDO:0005820

lassa virus infectious diseaseMondoMONDO:0044750

late congenital syphilisMondoMONDO:0005821

late infantile CACH syndromeMondoMONDO:0015520

late infantile neuronal ceroid lipofuscinosisMondoMONDO:0015674

late infantile neuronal ceroid lipofuscinosis 1MondoMONDO:0979340

late infantile neuronal ceroid lipofuscinosis 10MondoMONDO:0979372

late infantile neuronal ceroid lipofuscinosis 2MondoMONDO:0979344

late infantile neuronal ceroid lipofuscinosis 5MondoMONDO:0979348

late infantile neuronal ceroid lipofuscinosis 6MondoMONDO:0979367

late infantile neuronal ceroid lipofuscinosis 8MondoMONDO:0979370

late latent syphilisMondoMONDO:0040923

late yawsMondoMONDO:0001066

late-adult onset retinitis pigmentosaMondoMONDO:0009984

late-infantile/juvenile Krabbe diseaseMondoMONDO:0016090

late-onset combined immunodeficiency due to ICOSL deficiencyMondoMONDO:0979290

late-onset familial hypoaldosteronismMondoMONDO:0035321

late-onset focal dermal elastosisMondoMONDO:0016437

late-onset idiopathic chronic pancreatitisMondoMONDO:0981008

late-onset isolated ACTH deficiencyMondoMONDO:0016042

late-onset junctional epidermolysis bullosaMondoMONDO:0019309

late-onset localized junctional epidermolysis bullosa-intellectual disability syndromeMondoMONDO:0009177

late-onset nephronophthisisMondoMONDO:0019742

late-onset Parkinson diseaseMondoMONDO:0008199

late-onset retinal degenerationMondoMONDO:0011579

late-onset Steinert myotonic dystrophyMondoMONDO:0035650

latent autoimmune diabetes in adultsMondoMONDO:0850306

latent early syphilisMondoMONDO:0040922

latent syphilisMondoMONDO:0005822

latent tuberculosis infectionMondoMONDO:0040753

latent yawsMondoMONDO:0040925

lateral cystoceleMondoMONDO:0001885

lateral displacement of eyeMondoMONDO:0001510

lateral medullary syndromeMondoMONDO:0006827

lateral meningocele syndromeMondoMONDO:0007537

lateral myocardial infarctionMondoMONDO:0003677

lateral sclerosisMondoMONDO:0018155

lateral semicircular canal malformation, familial, with external and middle ear abnormalitiesMondoMONDO:0012133

lateral sinus thrombosisMondoMONDO:0002693

lateral ventricle meningiomaMondoMONDO:0003775

laterality defects, autosomal dominantMondoMONDO:0010991

latex allergyMondoMONDO:0000807

lathosterolosisMondoMONDO:0011816

lathyrismMondoMONDO:0043339

lattice corneal dystrophyMondoMONDO:0004686

lattice corneal dystrophy type IMondoMONDO:0007380

lattice degeneration of retina leading to retinal detachmentMondoMONDO:0007882

Laubry-Pezzi syndromeMondoMONDO:0020427

Laugier-Hunziker syndromeMondoMONDO:0023605

Laurence-Moon syndromeMondoMONDO:0009514

Laurence-Prosser-Rocker syndromeMondoMONDO:0023607

laurin-Sandrow syndromeMondoMONDO:0007615

LCA5-related retinopathyMondoMONDO:0100445

LCAT deficiencyMondoMONDO:0018999

le Marec-Bracq-Picaud syndromeMondoMONDO:0023609

lead poisoningMondoMONDO:0018019

learning disabilityMondoMONDO:0004681

Leber congenital amaurosisMondoMONDO:0018998

Leber congenital amaurosis 1MondoMONDO:0008764

Leber congenital amaurosis 10MondoMONDO:0012723

Leber congenital amaurosis 11MondoMONDO:0013454

Leber congenital amaurosis 12MondoMONDO:0012525

Leber congenital amaurosis 13MondoMONDO:0012990

Leber congenital amaurosis 14MondoMONDO:0013231

Leber congenital amaurosis 15MondoMONDO:0013457

Leber congenital amaurosis 16MondoMONDO:0013613

Leber congenital amaurosis 17MondoMONDO:0014145

Leber congenital amaurosis 18MondoMONDO:1060145

Leber congenital amaurosis 19MondoMONDO:0032794

Leber congenital amaurosis 2MondoMONDO:0008765

Leber congenital amaurosis 3MondoMONDO:0011415

Leber congenital amaurosis 4MondoMONDO:0011458

Leber congenital amaurosis 5MondoMONDO:0011473

Leber congenital amaurosis 6MondoMONDO:0013446

Leber congenital amaurosis 7MondoMONDO:0013449

Leber congenital amaurosis 8MondoMONDO:0013453

Leber congenital amaurosis 9MondoMONDO:0012056

Leber congenital amaurosis with early-onset deafnessMondoMONDO:0060650

Leber hereditary optic neuropathyMondoMONDO:0010788

Leber hereditary optic neuropathy, autosomal recessiveMondoMONDO:0030309

Leber optic atrophy and dystoniaMondoMONDO:0010772

Leber optic atrophy, susceptibility toMondoMONDO:0010640

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